US11421349B2 - Photoactivatable fibers and fabric media - Google Patents

Photoactivatable fibers and fabric media Download PDF

Info

Publication number
US11421349B2
US11421349B2 US15/523,283 US201515523283A US11421349B2 US 11421349 B2 US11421349 B2 US 11421349B2 US 201515523283 A US201515523283 A US 201515523283A US 11421349 B2 US11421349 B2 US 11421349B2
Authority
US
United States
Prior art keywords
photoactivatable
fibers
fiber
eosin
xanthene dye
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
US15/523,283
Other versions
US20170362744A1 (en
Inventor
Remigio Piergallini
Nikolaos Loupis
David Ohayon
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fle International Srl
Original Assignee
Klox Technologies Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Klox Technologies Inc filed Critical Klox Technologies Inc
Priority to US15/523,283 priority Critical patent/US11421349B2/en
Assigned to KLOX TECHNOLOGIES INC. reassignment KLOX TECHNOLOGIES INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LOUPIS, NIKOLAOS, OHAYON, DAVID, PIERGALLINI, REMIGIO
Publication of US20170362744A1 publication Critical patent/US20170362744A1/en
Application granted granted Critical
Publication of US11421349B2 publication Critical patent/US11421349B2/en
Assigned to FLE INTERNATIONAL S.R.L. reassignment FLE INTERNATIONAL S.R.L. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KLOX TECHNOLOGIES INC.
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F1/00General methods for the manufacture of artificial filaments or the like
    • D01F1/02Addition of substances to the spinning solution or to the melt
    • D01F1/10Other agents for modifying properties
    • D01F1/106Radiation shielding agents, e.g. absorbing, reflecting agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N5/0613Apparatus adapted for a specific treatment
    • A61N5/0616Skin treatment other than tanning
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N5/0613Apparatus adapted for a specific treatment
    • A61N5/062Photodynamic therapy, i.e. excitation of an agent
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/02Use of particular materials as binders, particle coatings or suspension media therefor
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
    • D06P1/0004General aspects of dyeing
    • D06P1/0012Effecting dyeing to obtain luminescent or phosphorescent dyeings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N2005/063Radiation therapy using light comprising light transmitting means, e.g. optical fibres
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N2005/0635Radiation therapy using light characterised by the body area to be irradiated
    • A61N2005/0643Applicators, probes irradiating specific body areas in close proximity
    • A61N2005/0645Applicators worn by the patient
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N2005/065Light sources therefor
    • A61N2005/0651Diodes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N2005/0658Radiation therapy using light characterised by the wavelength of light used
    • A61N2005/0659Radiation therapy using light characterised by the wavelength of light used infrared
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61NELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00Radiation therapy
    • A61N5/06Radiation therapy using light
    • A61N2005/0658Radiation therapy using light characterised by the wavelength of light used
    • A61N2005/0662Visible light
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds

Definitions

  • the present disclosure generally relates to photoactivatable fibers and fabric media comprising photoactivable agents, to methods of forming such photoactivatable fibers and fabric media, and to potential uses thereof.
  • Phototherapy has been recognized as having a wide range of applications in both the medical and cosmetic fields including use in surgery, therapy and diagnostics.
  • phototherapy has been used to treat cancers and tumors with lessened invasiveness, to disinfect target sites as an antimicrobial treatment, to treat skin conditions and to promote wound healing.
  • phototherapy has typically been achieved using photoactivatable formulations and/or composition comprising photoactivatable agents capable of absorbing and/or emitting light.
  • photoactivatable formulations and/or compositions have typically been prepared and/or used as liquids or semi-liquids (e.g., gels, pastes, creams and the like). Due to their liquid and/or semi-liquid texture, some of these photoactivatable formulations and/or compositions exhibit leaching of the photoactivating agents out of the formulations and/or compositions. Also, these formulations and/or compositions require a support/surface onto which they can be are applied.
  • the present disclosure relates to photoactivatable formulations having features that may present additional advantages over the photoactivatable formulations known to date. Such features may be useful in phototherapy and may contribute to a wider industrial applicability of the photoactivatable formulations.
  • the present disclosure relates to a photoactivatable fiber comprising: at least one thermoplastic polymer, and at least one photoactivatable agent; wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
  • the present disclosure relates to a photoactivatable fabric comprising a plurality of fibers composed of at least one thermoplastic polymer; and at least one photoactivatable agent, wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
  • the present disclosure relates to an article of manufacture comprising a photoactivatable fabric, wherein the photoactivatable fabric comprises: a) a plurality of fibers composed of at least one thermoplastic polymer; and b) at least one photoactivatable agent, wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
  • the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying a photoactivatable fiber as defined herein onto the subject; and illuminating the photoactivatable fiber with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
  • the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying a photoactivatable fabric as defined herein onto the subject; and illuminating the photoactivatable fabric with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
  • the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying an article of manufacture as defined herein onto the subject; and illuminating the article of manufacture with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
  • the present disclosure relates to the use of a photoactivatable fiber as defined herein for effecting phototherapy to a subject.
  • the present disclosure relates to the use of a photoactivatable fabric as defined herein for effecting phototherapy to a subject.
  • the present disclosure relates to the use of an article of manufacture as defined herein for effecting phototherapy to a subject.
  • the present disclosure relates to an article of manufacture comprising a first photoactivatable fabric; and a second photoactivatable fabric; wherein the first and second photoactivatable fabrics are associated with one another and comprise at least one photoactivatable agent that absorbs and emits light between about 400 nm and about 800 nm.
  • FIGS. 1A-1C illustrate a schematic representation of an extruder process used in the preparation of the photoactivatable fibers of the present disclosure.
  • FIG. 1B illustrates a picture of a cross-sectional view of fibers prepared by the extrusion process according to one embodiment of the present disclosure ( FIG. 1B showing the core of the fibers).
  • FIG. 1C illustrates a picture of a cross-sectional view of fibers prepared by extrusion process according to another embodiment of the present disclosure, wherein the fibers have a sheath and a core.
  • FIGS. 2A-2D illustrate graphs showing the fluorescence emission over time of a photoactivatable agent present in nylon fibers ( FIG. 2A ), PBT fibers ( FIG. 2B ), and PMMA fibers ( FIG. 2C ).
  • FIG. 2D illustrates a graph comparing the effect of the polymers tested on fluorescence emission over time of the photoactivatable agents.
  • FIG. 3 illustrates a graph comparing the leaching of Eosin out of the indicated photoactivatable fibers according to one embodiment of the present disclosure.
  • FIG. 4 illustrates a graph showing the effect of addition of a lubricant to fluorescence emission by Eosin Y in solution.
  • FIGS. 5A-5B illustrate a graph showing the effect of the presence of a lubricant on fluorescence emission of different concentrations of Eosin Y.
  • FIG. 5B illustrates a graph comparing the effect of the presence of a lubricant on fluorescence emission of Eosin Y and on fluorescence emission of fluorescein.
  • FIGS. 6A-6B illustrate a graph comparing the fluorescence emission over time of a photoactivatable polypropylene fiber according to the present disclosure having 2, 4 or 6 layers of a EosinY:fluorescein composition on its surface.
  • FIG. 6B illustrates a graph comparing the fluorescence emission over time of a photoactivatable nylon fiber according to an embodiment of the present disclosure having 2, 4 or 6 layers of a fluorescein composition on its surface.
  • FIG. 7 illustrates a graph comparing the fluorescence emission of over time of photoactivatable nylon fibers according to one embodiment of the present disclosure having the photoactivatable agent present inside of the photoactivatable nylon fibers (inner) or on the surface (outer).
  • FIGS. 8A-8F illustrate pictures of the fluorescence emission of photoactivatable polypropylene fibers according to one embodiment of the present disclosure which were dipped in a solution of Eosin Y (0.1 g/L).
  • FIGS. 8A and 8B show the fluorescence emission under blue lamp after one day wherein the fibers were not emerged in water.
  • FIGS. 8C and 8D show the fluorescence emission under blue lamp after three days wherein the fibers were not emerged in water.
  • FIGS. 8E and 8F show the fluorescence emission under blue lamp after three days emerged in water.
  • FIGS. 9A-9P illustrate pictures of the fluorescence emission under blue lamp of fibers dipped in a solution of photoactivatable agents, i.e., commercial dental fibers in Eosin Y 50 g/L ( FIGS. 9A-9B ); commercial dental fibers in Eosin Y 0.1 g/L ( FIGS. 9C-9D ); commercial dental fibers in fluorescein 50 g/L ( FIGS. 9E-19F ), commercial dental fibers in fluorescein 0.1 g/L ( FIGS. 9G-9H ), commercial dental fibers in fluorescein:Eosin Y 50 g/L ( FIG.
  • FIGS. 9I-9J commercial dental fibers in fluorescein:Eosin Y 0.1 g/L ( FIGS. 9K-9L ), polypropylene fibers in fluorescein 50 g/L ( FIGS. 9M-9N ), polypropylene fibers in fluorescein 0.1 g/L ( FIGS. 9O-9P ).
  • FIG. 10 illustrates a schematic representation of a process for the preparation of photoactivatable fabrics according to one embodiment of the present disclosure.
  • FIGS. 11A-11B illustrate a schematic representation of an article of manufacture, in occurrence a suit-like garment, according to one embodiment of the present disclosure.
  • FIG. 11B illustrates a picture of a suit-like garment prepared with the photoactivatable fabrics according to one embodiment of the present disclosure.
  • the present disclosure relates to fibers and fabric media comprising photoactivatable agents and to fibers and fabric media that are photoactivatable by photoactivation of the photoactivatable agents.
  • the fibers and the fabric media have photoactivatable agents present on their surface (e.g., the fiber/fabric is coated or sprayed with the photoactivatable agents or the fiber/fabric is dipped into a composition or a formulation comprising the photoactivatable agent).
  • the photoactivatable agents are incorporated into the materials making the fibers (e.g., the photoactivatable agents are mixed/compounded with the materials making the fibers).
  • the photoactivatable agents are present both on the surface of the fiber/fabric and incorporated/compounded into the materials making the fibers.
  • the fibers are, but not limited to, synthetic fibers, natural fibers, and textile fibers.
  • synthetic fibers may be made from a polymer or a combination of different polymers.
  • the polymer is a thermoplastic polymer.
  • fiber relates to a string or a thread or a filament used as a component of composite materials. Fibers may be used in the manufacture of other materials such as for example, but not limited to, fabrics.
  • the polymer is acrylic, acrylonitrile butadiene styrene (ABS), polybenzimidazole (PBI), polycarbonate, polyether sulfone (PES), polyetherether ketone (PEEK), polyetherimide (PEI), polyethylene (PE), polyphenylene oxide (PPO), polyphenylene sulfide (PPS), polypropylene (PP), polystyrene, polyvinyl chloride (PVC), teflon, polybutylene, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), nylon, polylactic acid (PLA), polymethyl methacrylate polyester, polyurethane, rayons, poly(methyl methacrylate) (PMMA), or from any mixture thereof.
  • ABS acrylonitrile butadiene styrene
  • PBI polybenzimidazole
  • PES polyether sulfone
  • PEEK polyetherether ketone
  • PEI poly
  • the fibers may be made from glycolic acid, copolymer lactide/glycolide, polyester polymer, copolymer polyglycolic acid/trimethylene carbonate, natural protein fiber, cellulose fiber, polyamide polymer, polymer of polypropylene, polymer of polyethylene, nylon, polymer of polylactic acid, polymer of polybutylene terephthalate, polyester, copolymer polyglycol, polybutylene, polymer of poly methyl methacrylate, or from any mixture thereof.
  • the fibers of the present disclosure may be coextruded fibers that have two distinct polymers forming the fiber, usually as a core-sheath or side-by-side.
  • the fibers may be composed of a single strand (mono-filament) or may be composed of a plurality of strands (multi-filaments).
  • the photoactivatable fibers that are multifilament may also be intertwined or braided or twisted (i.e., the multifilaments are intertwined, braided or twisted to form the fibers).
  • the diameter of the photoactivatable fiber define herein varies between about 15 microns and about 500 microns, between about 25 microns and about 500 microns, between about 50 microns and 400 microns, between about 50 microns and about 300 microns, preferably between about 50 microns and about 250 microns, preferably between about 75 microns and about 300 microns, and most preferably between about 75 microns and about 250 microns.
  • the diameter of the photoactivatable fibers defined herein is about 15 microns, about 20 microns, about 25 microns, about 50 microns, about 75 microns, about 100 microns, about 125 microns, about 150 microns, about 175 microns, about 200 microns, about 225 microns, about 250 microns, about 250 microns, about 275 microns, about 300 microns, about 325 microns, about 350 microns, about 375 microns, about 400 microns, about 425 microns, about 450 microns, about 475 microns, about 500 microns. In some instances, the diameter of the photoactivatable fibers defined herein (taken individually) is about 31 microns.
  • the photoactivatable fibers defined herein show a medium to high resistance to mechanical pulling and stretching forces. In some implementations, the photoactivatable fibers defined here are resilient and have the ability to stretch and to reform to their original size and shape.
  • the photoactivatable fibers have a linear mass density of between about 400 and about 480 Deniers, between about 410 and about 470 Deniers, between about 420 and about 460 Deniers, between about 420 and about 450 Deniers, or about 428 Deniers.
  • the term “Denier” refers to a unit of measure for the linear mass density of fibers, is defined as the mass in grams per 9000 meters.
  • the fibers defined herein maintain their length and degree of flexibility and windability.
  • the stretch fibers may be lubricated to wind and unwind without damage being inflicted on the fibers due to the winding and the unwinding process.
  • the fibers have a tensile strength that allows the fibers to be stretched so as to reach a minimum diameter at least half, one third, one fourth, one fifth, one sixth, one seventh, one eight, one ninth, or one tenth of the original diameter.
  • FIG. 1A illustrates is a schematic representation of an example of a process for preparing photoactivatable fibers according to one embodiment of the present disclosure.
  • an extrusion process is used wherein polymer pellets are melted and extruded and then pulled into a fiber while still hot.
  • a solution of photoactivatable agents in water and oil is sprayed onto the polymer while it is still hot.
  • the fibers are then spun onto a bobbin for storage and ease of use.
  • the photoactivatable fibers of the present disclosure are prepared using a TEM co-rotating twin screw extruder.
  • the photoactivatable agent is a chemical compound which, when exposed to the light is photoexcited and can then transfer its energy to other molecules or emit it as light, such as for example fluorescence.
  • the photoactivable agent when photoexcited by the light may transfer its energy to enhance or accelerate light dispersion or to other molecules such as oxidants to release oxygen radicals.
  • photoactivable agents include, but are not limited to, fluorescent compounds (or stains) (also known as “fluorochromes” or “fluorophores” or “chromophores”).
  • Other dye groups or dyes biological and histological dyes, food colorings, carotenoids, and other dyes
  • Suitable photoactivatable agent can be those that are Generally Regarded As Safe (GRAS).
  • the photoactivatable fibers of the present disclosure comprise a first photoactivatable agent.
  • the first photoactivatable agent absorbs at a wavelength in the range of the visible spectrum, such as at a wavelength of about 380 nm to about 800 nm, about 380 nm to about 700, about 400 nm to about 800, or about 380 nm to about 600 nm.
  • the first photoactivating agent absorbs at a wavelength of about 200 nm to about 800 nm, of about 200 nm to about 700 nm, of about 200 nm to about 600 nm or of about 200 nm to about 500 nm.
  • the first photoactivatable agent absorbs at a wavelength of about 200 nm to about 600 nm. In some embodiments, the first photoactivatable agent absorbs light at a wavelength of about 200 nm to about 300 nm, of about 250 nm to about 350 nm, of about 300 nm to about 400 nm, of about 350 nm to about 450 nm, of about 400 nm to about 500 nm, of about 450 nm to about 650 nm, of about 600 nm to about 700 nm, of about 650 nm to about 750 nm or of about 700 nm to about 800 nm.
  • the photoactivatable agents emit light within the range of about 400 nm and about 800 nm.
  • the photoactivatable fibers disclosed herein may include at least one additional photoactivatable agent.
  • Combining photoactivatable agents may increase photo-absorption by the combined dye molecules and enhance absorption and photo-biomodulation selectivity.
  • the photoactivatable fibers of the disclosure include more than one photoactivatable agent.
  • photoactivatable fibers have the photoactivatable agent on their surface (i.e., the surface of the fibers that is in contact with the surrounding environment of the fiber)
  • photoactivatable fibers may be prepared by being dipped into a photoactivatable agent composition comprising one or more photoactivatable agents and a carrier material such as, but not limited to, water.
  • such photoactivatable fibers may be prepared by being sprayed with a photoactivatable agent composition comprising one or more photoactivatable agents and a carrier material.
  • the photoactivatable agent composition has a consistency that allows the fibers to be dipped into the composition. In some specific examples, the photoactivatable agent composition is in a liquid or semi-liquid form.
  • the carrier material may be any liquid or semi liquid material that is compatible with the photoactivatable agent that is any material that does not affect the photoactive properties of the photoactivatable agent, such as, for example, water.
  • the photoactivatable agent composition has a consistency that allows the photoactivatable agent composition to be sprayed onto the fibers.
  • the photoactivatable fibers are prepared by incorporating the photoactivatable agent into the fiber composition.
  • the photoactivatable fibers are prepared by extrusion.
  • the photoactivatable fibers are prepared by a process which uses spinning. The spinning may be wet, dry, dry jet-wet, melt, gel, or electrospinning. The polymer being spun may be converted into a fluid state. If the polymer is a thermoplastic then it may be melted, otherwise it may be dissolved in a solvent or may be chemically treated to form soluble or thermoplastic derivatives.
  • the molten polymer is then forced through the spinneret, and then it cools to a rubbery state, and then a solidified state. If a polymer solution is used, then the solvent is removed after being forced through the spinneret.
  • a composition of the photoactivatable agent may be added to the polymer in the fluid state or to the melted polymer or to the polymer dissolved into a solvent. Melt spinning may be used for polymers that can be melted. The polymer having the photoactivatable agents dispersed therein solidifies by cooling after being extruded from the spinneret.
  • the photoactivatable agent may be uniformly or a non-uniformly distributed within the photoactivatable fibers.
  • concentration of photoactivatable agent in the photoactivatable fibers is steady as the photoactivatable fibers disintegrate, whereas when the photoactivatable agent is not uniformly distributed within the photoactivatable fibers, the concentration of the photoactivatable agent in the photoactivatable fibers varies as the photoactivatable fibers disintegrate.
  • the concentration of the photoactivatable agent to be used may be selected based on the desired intensity and duration of the photoactivity to be emitted from the photoactivatable fibers, and on the desired phototherapeutic, medical or cosmetic effect. For example, some dyes such as xanthene dyes reach a ‘saturation concentration’ after which further increases in concentration do not provide substantially higher emitted fluorescence. Further increasing the photoactivatable agent concentration above the saturation concentration can reduce the amount of activating light passing through the photoactivatable fibers. Therefore, if more fluorescence is required for a certain application than activating light, a high concentration of photoactivatable agent can be used. However, if a balance is required between the emitted fluorescence and the activating light, a concentration close to or lower than the saturation concentration can be chosen.
  • Suitable photoactivatable agent that may be used in the photoactivatable fibers of the present disclosure include, but are not limited to the following:
  • Chlorophyll dyes include but are not limited to chlorophyll a; chlorophyll b; chlorophyllin; bacteriochlorophyll a; bacteriochlorophyll b; bacteriochlorophyll c; bacteriochlorophyll d; protochlorophyll; protochlorophyll a; amphiphilic chlorophyll derivative 1; and amphiphilic chlorophyll derivative 2.
  • Xanthene derivatives—xanthene dyes include but are not limited to eosin, eosin B (4′,5′-dibromo, 2′,7′-dinitr-o-fluorescein, dianion); eosin Y; eosin Y (2′,4′,5′,7′-tetrabromo-fluorescein, dianion); eosin (2′,4′,5′,7′-tetrabromo-fluorescein, dianion); eosin (2′,4′,5′,7′-tetrabromo-fluorescein, dianion); eosin (2′,4′,5′,7′-tetrabromo-fluorescein, dianion) methyl ester; eosin (2′,4′,5′,7′-tetrabromo-fluorescein, monoanion) p-is
  • Methylene blue dyes include, but are not limited to, 1-methyl methylene blue; 1,9-dimethyl methylene blue; methylene blue; methylene blue (16 ⁇ M); methylene blue (14 ⁇ M); methylene violet; bromomethylene violet; 4-iodomethylene violet; 1,9-dimethyl-3-dimethyl-amino-7-diethyl-a-mino-phenothiazine; and 1,9-dimethyl-3-diethylamino-7-dibutyl-amino-phenot-hiazine.
  • Azo dyes include but are not limited to methyl violet, neutral red, para red (pigment red 1), amaranth (Azorubine S), Carmoisine (azorubine, food red 3, acid red 14), allura red AC (FD&C 40), tartrazine (FD&C Yellow 5), orange G (acid orange 10), Ponceau 4R (food red 7), methyl red (acid red 2), and murexide-ammonium purpurate.
  • the one or more photoactivatable agents of the photoactivatable fibers disclosed herein can be independently selected from any of Acid black 1, Acid blue 22, Acid blue 93, Acid fuchsin, Acid green, Acid green 1, Acid green 5, Acid magenta, Acid orange 10, Acid red 26, Acid red 29, Acid red 44, Acid red 51, Acid red 66, Acid red 87, Acid red 91, Acid red 92, Acid red 94, Acid red 101, Acid red 103, Acid roseine, Acid rubin, Acid violet 19, Acid yellow 1, Acid yellow 9, Acid yellow 23, Acid yellow 24, Acid yellow 36, Acid yellow 73, Acid yellow S, Acridine orange, Acriflavine, Alcian blue, Alcian yellow, Alcohol soluble eosin, Alizarin, Alizarin blue 2RC, Alizarin carmine, Alizarin cyanin BBS, Alizarol cyanin R, Alizarin red S, Alizarin purpurin, Aluminon, Amido black 10B, Amidoschwarz, Aniline blue WS, An
  • the photoactivatable fibers of the present disclosure may include any of the photoactivatable agents listed above, or a combination thereof, so as to provide a synergistic biophotonic effect.
  • the following synergistic combinations of photoactivatable agents may be used: Eosin Y and Fluorescein; Fluorescein and Rose Bengal; Erythrosine in combination with Eosin Y, Rose Bengal or Fluorescein; Phloxine B in combination with one or more of Eosin Y, Rose Bengal, Fluorescein and Erythrosine; Eosin Y, Fluorescein and Rose Bengal.
  • the photoactivatable agent is present in the photoactivatable agent composition at a concentration of about 100 g/L, about 50 g/L, about 10 g/L, about 5 g/L, about 1 g/L or about 0.1 g/L of the total volume.
  • the photoactivatable agent is present in the photoactivatable agent composition at a concentration of between about 10 g/L and about 100 g/L.
  • the photoactivatable agent is present in the photoactivatable agent composition at a concentration that is lower than 0.1 g/L, for example, the photoactivatable agent is present in the photoactivatable agent composition at a concentration in the milligram/L or in the microgram/L range.
  • the photoactivatable fibers of the present disclosure comprise a lubricant.
  • the lubricant is coated onto the photoactivatable fibers of the present disclosure.
  • the lubricant is treatment oil, such as but not limited to Polyethylene glycol esters (e.g., Lurol OilTM).
  • the addition of a lubricant to the surface of the fibers improves the retention of the composition of photoactivatable agents onto the fibers.
  • the lubricant improves the hydrophilicity of the polymer so that it increases the absorption of the solution of photoactivatable agent.
  • leaching of the photoactivatable agent out of the photoactivatable fibers of the present disclosure may be assessed by placing 0.1 g of the photoactivatable fibers in 10 ml of water for 1 day and by then measuring the amount of photoactivatable agent in the water.
  • the photoactivatable fibers as defined herein may be woven into a fabric material resulting in a photoactivatable fabric comprising a plurality of photoactivatable fibers.
  • the photoactivatable fabric comprising the photoactivatable fibers exhibits substantially no leaching of the photoactivatable agent.
  • the term “fabric” relates to a woven material composed of a network of fibers or to a non-woven (e.g., spunbound) material composed of fibers.
  • Weaving is a method of textile production in which two distinct sets of yarns or threads are interlaced at right angles to form a fabric or cloth. Similar methods are knitting, felting, and braiding or plaiting.
  • Non-woven fabrics are broadly defined as sheet or web structures bonded together by entangling fiber or filaments mechanically, thermally or chemically. They are flat or tufted porous sheets that are made directly from separate fibers, molten plastic or plastic film. They are not made by weaving or knitting and do not require converting the fibers to yarn.
  • the fabric material may be used in the fabrication of an article of manufacture such as, but not limited to, a garment, an article of clothing, a wound dressing, a towel, bedding, and the like.
  • the garment may be a shirt, pants, glove, mask, socks, or the like.
  • the photoactivatable fibers of the present disclosure are woven into a fabric material is a suit or a suit-like garment.
  • the fabric made from such fibers is also photoactivatable.
  • the fabric made from such fibers may be coated or dipped or sprayed with a photoactivatable agent composition to render the fabric photoactivatable.
  • the photoactivatable fabric may be a nonwoven photoactivatable fabric such as but not limited to a spunbound fabric.
  • Spunbond fabrics may be produced by depositing extruded, spun filaments onto a collecting belt in a uniform random manner followed by bonding the fibers. The fibers may be separated during the web laying process by air jets or electrostatic charges. The collecting surface is usually perforated to prevent the air stream from deflecting and carrying the fibers in an uncontrolled manner. Bonding imparts strength and integrity to the web by applying heated rolls or hot needles to partially melt the polymer and fuse the fibers together.
  • high molecular weight and broad molecular weight distribution polymers such as, but not limited to, polypropylene, polyester, polyethylene, polyethylene terephthalate, nylon, polyurethane, and rayons may be used in the manufacture of spunbound fabrics.
  • spunbound fabrics may be composed of a mixture of polymers.
  • a lower melting polymer can function as the binder which may be a separate fiber interspersed with higher melting fibers, or two polymers may be combined into a single fiber type. In the latter case the so-called bi-component fibers possess a lower melting component, which acts as a sheath covering over a higher melting core. Bicomponent fibers may also spun by extrusion of two adjacent polymers.
  • spunbonding may combine fiber spinning with web formation by placing the bonding device in line with spinning.
  • the web may be bonded in a separate step.
  • the spinning process may be similar to the production of continuous filament yarns and may utilize similar extruder conditions for a given polymer. Fibers are formed as the molten polymer exits the spinnerets and is quenched by cool air. The objective of the process is to produce a wide web and, therefore, many spinnerets are placed side by side to generate sufficient fibers across the total width.
  • the output of a spinneret Before deposition on a moving belt or screen, the output of a spinneret usually includes a plurality of individual filaments which must be attenuated to orient molecular chains within the fibers to increase fiber strength and decrease extensibility. This is accomplished by rapidly stretching the plastic fibers immediately after exiting the spinneret. In practice the fibers are accelerated either mechanically or pneumatically.
  • the web is formed by the pneumatic deposition of the filament bundles onto the moving belt.
  • a pneumatic gun uses high-pressure air to move the filaments through a constricted area of lower pressure, but higher velocity as in a venturi tube. In order for the web to achieve maximum uniformity and cover, individual filaments are separated before reaching the belt.
  • the belt is usually made of an electrically grounded conductive wire. Upon deposition, the belt discharges the filaments. Webs produced by spinning linearly arranged filaments through a so-called slot die eliminating the need for such bundle separating devices.
  • the photoactivatable fabrics of the present disclosure preferably have a thickness that allows light to reach the photoactivatable agents embedded in the fibers of the fabric and for the light emitted by the photoactivatable agents to exit the fabric.
  • the photoactivatable fibers and the photoactivatable fabrics of the present disclosure may have cosmetic and/or medical benefits.
  • the photoactivatable fibers and the photoactivatable fabrics may be used to promote prevention and/or treatment of a tissue or an organ and/or to treat a tissue or an organ of a subject in need of phototherapy.
  • the photoactivatable fibers and/fabrics of the present disclosure may be used to promote treatment of a skin disorder such as acne, eczema, dermatitis or psoriasis, promote tissue repair, and modulate inflammation, modulate collagen synthesis, reduce or avoid scarring, for cosmesis, or promote wound healing. They can be used to treat acute inflammation.
  • Acute inflammation can present itself as pain, heat, redness, swelling and loss of function, and includes inflammatory responses such as those seen in allergic reactions such as those to insect bites e.g.; mosquito, bees, wasps, poison ivy, or post-ablative treatment.
  • the photoactivatable fibers and/fabrics of the present disclosure may provide treatment of a skin disorder, preventing or treating scarring, and/or accelerating wound healing and/or tissue repair.
  • the photoactivatable fibers or fabrics may be used to promote wound healing.
  • the photoactivatable fibers or fabrics may be applied at wound site as deemed appropriate by the physician or other health care providers.
  • the photoactivatable fibers or fabrics may be used following wound closure to optimize scar revision.
  • the photoactivatable fibers or fabrics may be applied at regular intervals such as once a week, or at an interval deemed appropriate by the physician or other health care providers.
  • the photoactivatable fibers or fabrics may be used following acne treatment to maintain the condition of the treated skin.
  • the photoactivatable fibers or fabrics may be applied at regular intervals such as once a week, or at an interval deemed appropriate by the physician or other health care providers.
  • the photoactivatable fibers or fabrics may be used following ablative skin treatment to maintain the condition of the treated skin.
  • the photoactivatable fibers or fabrics of the present disclosure may be used to treat skin disorders that include, but are not limited to, erythema, telangiectasia, actinic telangiectasia, basal cell carcinoma, contact dermatitis, dermatofibrosarcoma protuberans, genital warts, hidradenitis suppurativa, melanoma, merkel cell carcinoma, nummular dermatitis, molloscum contagiosum, psoriasis, psoriatic arthritis, rosacea, scabies, scalp psoriasis, sebaceous carcinoma, squamous cell carcinoma, seborrheic dermatitis, seborrheic keratosis, shingles, tinea versicolor, warts, skin cancer, pemphigus, sunburn, dermatitis, eczema, rashes, impetigo, lichen simplex chronicus, rhinophyma
  • Dermatitis includes contact dermatitis, atopic dermatitis, seborrheic dermatitis, nummular dermatitis, generalized exfoliative dermatitis, and statis dermatitis.
  • Skin cancers include melanoma, basal cell carcinoma, and squamous cell carcinoma.
  • the photoactivatable fibers or fabrics of the present disclosure may be used to treat acne.
  • acne means a disorder of the skin caused by inflammation of skin glands or hair follicles.
  • the photoactivatable fibers or fabrics of the disclosure can be used to treat acne at early pre-emergent stages or later stages where lesions from acne are visible. Mild, moderate and severe acne can be treated with embodiments of photoactivatable fibers or fabrics.
  • Early pre-emergent stages of acne usually begin with an excessive secretion of sebum or dermal oil from the sebaceous glands located in the pilosebaceous apparatus. Sebum reaches the skin surface through the duct of the hair follicle.
  • the photoactivatable fibers or fabrics of the present disclosure can be used to treat one or more of skin irritation, pitting, development of scars, comedones, inflammatory papules, cysts, hyperkeratinazation, and thickening and hardening of sebum associated with acne.
  • Some skin disorders present various symptoms including redness, flushing, burning, scaling, pimples, papules, pustules, comedones, macules, nodules, vesicles, blisters, telangiectasia, spider veins, sores, surface irritations or pain, itching, inflammation, red, purple, or blue patches or discolorations, moles, and/or tumors.
  • the photoactivatable fibers or fabrics of the present disclosure may be used to treat various types of acne.
  • Some types of acne include, for example, acne vulgaris, cystic acne, acne atrophica, bromide acne, chlorine acne, acne conglobata, acne cosmetica, acne detergicans, epidemic acne, acne estivalis, acne fulminans, halogen acne, acne indurata, iodide acne, acne keloid, acne mechanica, acne papulosa, pomade acne, premenstral acne, acne pustulosa, acne scorbutica, acne scrofulosorum, acne urticata, acne varioliformis, acne venenata, propionic acne, acne excoriee, gram negative acne, steroid acne, and nodulocystic acne.
  • the photoactivatable fibers or fabrics of the present disclosure are used in conjunction with systemic or topical antibiotic treatment.
  • antibiotics used to treat acne include tetracycline, erythromycin, minocycline, doxycycline.
  • the article of manufacture being composed of the photoactivatable fabric of the present disclosure may have an anti-infective effect, for example when used in the treatment of a wound to prevent infection and/or re-infection of the wound by bacteria or by other infective agents.
  • the photoactivatable fibers or fabrics of the present disclosure may be used to treat wounds, promote wound healing, promote tissue repair and/or prevent or reduce cosmesis including improvement of motor function (e.g. movement of joints).
  • Wounds that may be treated by the photoactivatable fibers and fabrics of the present disclosure include, for example, injuries to the skin and subcutaneous tissue initiated in different ways (e.g., pressure ulcers from extended bed rest, wounds induced by trauma or surgery, burns, ulcers linked to diabetes or venous insufficiency) and with varying characteristics.
  • the present disclosure provides photoactivatable fibers or fabrics for treating and/or promoting the healing of, for example, burns, incisions, excisions, lesions, lacerations, abrasions, puncture or penetrating wounds, surgical wounds, contusions, hematomas, crushing injuries, amputations, sores and ulcers.
  • the photoactivatable fibers and fabrics of the present disclosure may be used in a method for effecting phototherapy on a subject, such as on a tissue and/or an organ of the subject.
  • a method for effecting phototherapy on a subject comprises the step of applying a photoactivatable fibers and fabric as defined herein onto the subject or onto the tissue or the organ in need of phototherapy and the step of illuminating the photoactivatable fiber and fabric with light having a wavelength that overlaps with that overlaps with an absorption spectrum of the photoactivatable agent.
  • the photoactivatable fibers and fabrics of the present disclosure may be used in phototherapy and/or in biophotonic therapy. In certain instances, the photoactivatable fibers and fabrics of the present disclosure may be used as biophotonic medical devices.
  • the photoactivatable fibers and fabrics of the present disclosure may be used in the manufacture of medical devices such as suture materials, stents, catheter, balloons, wound dressing or the like.
  • the photoactivatable fibers may be used in the fabrication of dental care devices such as in the fabrication of toothbrush, dental floss, braces and the like.
  • the methods of the present disclosure comprise applying a photoactivatable fiber or photoactivatale fabric of the present disclosure to a tissue or organ in need of phototherapy and illuminating the photoactivatable fiber or photoactivatale fabric with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent(s) present in the photoactivatable fiber or photoactivatable fabric to induce emission of the photoactivatable agent(s).
  • any source of actinic light can be used. Any type of halogen, LED or plasma arc lamp, or laser may be suitable.
  • the primary characteristic of suitable sources of actinic light will be that they emit light in a wavelength (or wavelengths) appropriate for activating the one or more photoactivatable agent present in the composition.
  • an argon laser is used.
  • a potassium-titanyl phosphate (KTP) laser e.g. a GreenLightTM laser
  • a LED lamp such as a photocuring device is the source of the actinic light.
  • the source of the actinic light is a source of light having a wavelength between about 200 to 800 nm.
  • the source of the actinic light is a source of visible light having a wavelength between about 400 and 600 nm. In another embodiment, the source of the actinic light is a source of visible light having a wavelength between about 400 and 700 nm. In yet another embodiment, the source of the actinic light is blue light. In yet another embodiment, the source of the actinic light is red light. In yet another embodiment, the source of the actinic light is green light. Furthermore, the source of actinic light should have a suitable power density. Suitable power density for non-collimated light sources (LED, halogen or plasma lamps) are in the range from about 0.1 mW/cm 2 to about 200 mW/cm 2 . Suitable power density for laser light sources are in the range from about 0.5 mW/cm 2 to about 0.8 mW/cm 2 .
  • the light has an energy at the subject's skin surface of between about 0.1 mW/cm 2 and about 500 mW/cm 2 , or 0.1-300 mW/cm 2 , or 0.1-200 mW/cm 2 , wherein the energy applied depends at least on the condition being treated, the wavelength of the light, the distance of the skin from the light source and the thickness of the photoactivatable fibers or fabrics.
  • the light at the subject's skin is between about 1-40 mW/cm 2 , or between about 20-60 mW/cm 2 , or between about 40-80 mW/cm 2 , or between about 60-100 mW/cm 2 , or between about 80-120 mW/cm 2 , or between about 100-140 mW/cm 2 , or between about 30-180 mW/cm 2 , or between about 120-160 mW/cm 2 , or between about 140-180 mW/cm 2 , or between about 160-200 mW/cm 2 , or between about 110-240 mW/cm 2 , or between about 110-150 mW/cm 2 , or between about 190-240 mW/cm 2 .
  • the activation of the photoactivatable agents may take place almost immediately on illumination (femto- or pico seconds). A prolonged exposure period may be beneficial to exploit the synergistic effects of the absorbed, reflected and reemitted light of the photoactivatable fibers and fabrics of the present disclosure and its interaction with the tissue being treated.
  • the time of exposure of photoactivatable fibers or fabrics to actinic light is a period between 0.01 minutes and 90 minutes.
  • the time of exposure of the photoactivatable fibers or fabrics to actinic light is a period between 1 minute and 5 minutes.
  • the photoactivatable fibers or fabrics are illuminated for a period between 1 minute and 3 minutes.
  • light is applied for a period of about 1-30 seconds, about 15-45 seconds, about 30-60 seconds, about 0.75-1.5 minutes, about 1-2 minutes, about 1.5-2.5 minutes, about 2-3 minutes, about 2.5-3.5 minutes, about 3-4 minutes, about 3.5-4.5 minutes, about 4-5 minutes, about 5-10 minutes, about 10-15 minutes, about 15-20 minutes, or about 20-30 minutes.
  • the treatment time may range up to about 90 minutes, about 80 minutes, about 70 minutes, about 60 minutes, about 50 minutes, about 40 minutes or about 30 minutes. It will be appreciated that the treatment time can be adjusted in order to maintain a dosage by adjusting the rate of fluence delivered to a treatment area.
  • the delivered fluence may be about 4 to about 60 J/cm 2 , 4 to about 90 J/cm 2 , 10 to about 90 J/cm 2 , about 10 to about 60 J/cm 2 , about 10 to about 50 J/cm 2 , about 10 to about 40 J/cm 2 , about 10 to about 30 J/cm 2 , about 20 to about 40 J/cm 2 , about 15 J/cm 2 to 25 J/cm 2 , or about 10 to about 20 J/cm 2 .
  • the photoactivatable fibers and photoactivatable fabric may be re-illuminated at certain intervals.
  • the source of actinic light is in continuous motion over the treated area for the appropriate time of exposure.
  • the photoactivatable fibers or photoactivatable fabric may be illuminated until the photoactivatable fibers or photoactivatable fabric is at least partially photobleached or fully photobleached.
  • the photoactivatable agents in the photoactivatable fibers or fabrics can be photoexcited by ambient light including from the sun and overhead lighting.
  • the photoactivatable agents can be photoactivated by light in the visible range of the electromagnetic spectrum.
  • the light can be emitted by any light source such as sunlight, light bulb, an LED device, electronic display screens such as on a television, computer, telephone, mobile device, flashlights on mobile devices.
  • any source of light can be used.
  • Ambient light can include overhead lighting such as LED bulbs, fluorescent bulbs, and indirect sunlight.
  • the photoactivatable fibers or fabric may be removed from the tissue or organ following application of light.
  • the photoactivatable fibers or fabric may be left on the tissue or organ for an extended period of time and re-activated with direct or ambient light at appropriate times to treat the condition.
  • Chromophores were incorporated into fibers made of polymer materials (polymer materials compounded with chromophores). The compounding involved taking a polymer melt and adding the chromophores in their solid form directly to the polymer, and then allowing the melt to cool. This process allowed chromophores to be integrated with the polymer fibers.
  • the polymer fibers were selected from fibers, nonwoven fabrics, tubes and films.
  • the chromophore to polymer ratio was selected so as to be dependent on the chromophore used, for example: for Eosin Y, 20% w/w ratio (in water) was used for the master chromophore batch, for Fluorescein, 5% w/w ratio was used for the master chromophore batch.
  • a pure Eosin Y fiber was made and a 4:1 mixture (by weight (or 1:1 by fiber weight)) of Eosin Y and Fluorescein was made.
  • Fibers made of polypropylene, of polyethylene, nylon, or of a combination thereof were prepared. Eosin Y or fluorescein or a combination of Eosin Y and fluorescein were used as photoactivatable agents.
  • a cross-sectional view of the fibers prepared using one type of polymer is shown in FIG. 1B .
  • the polyethylene was made into a 50/50 polyethylene core with a polypropylene sheath.
  • a cross-sectional view of these fibers is shown in FIG. 1C .
  • Fibers having the following composition have been considered:
  • Polypropylene fibers were used as non-woven samples. The following fibers were prepared:
  • Fibers were dipped in a bath of chromophore and lubricant (1:6 oil:water) (i.e., lurol oil) to produce fibers that were colored and that fluoresced.
  • the fibers incorporated two chromophores, both Eosin Y and a fluorescein/Eosin Y mixture (1/4).
  • the polyethylene was made into a 50/50 polyethylene core with a polypropylene sheath.
  • Fibers having the following composition have been considered:
  • the photoactivatable fibers outlined in Tables 1, 5, 9, 14, 19 and 25 were prepared; a composition of photoactivatable agents was sprayed onto some of the fibers. Each of these fibers was assessed for its ability to emit fluorescence following illumination for 5 mins at 5 cm using a TheraTM Lamp.
  • the results are presented in FIG. 2A (nylon fibers), FIG. 2B (PBT fibers) and FIG. 2C (PMMA fibers) and in Tables 2, 3, 4, 6, 7, 8, 10, 11, 12, 13, 15, 16, 17, 18, 20, 21, 22, 23, 24, 26, 27, 28, 29, 30, 31, 32 and 33.
  • Photoactivatable fibers comprising polyethylene compounded with Eosin Fluorescence Fiber Composition Emission 1 Polyethylene with 0.5% Eosin + Lurol Oil Coating Table 2 2 Polyethylene with 0.5% Eosin + 1% Urea Peroxide Table 3 Coating + Lurol Oil Coating 3 Polyethylene with 0.5% Eosin + Sodium Table 4 Bicarbonate Coating + Lurol Oil Coating 4 Polyethylene with 0.5% Eosin + 10 g/L Eosin Y — Coating + Lurol Oil Coating
  • Photoactivatable fibers comprising polylactic acid (PLA) compounded with Eosin Fluorescence Fiber Composition Emission 5 PLA with 0.5% Eosin + Lurol Oil Coating Table 6 6 PLA with 0.5% Eosin + 1% Urea Peroxide Table 7 Coating + Lurol Oil Coating 7 PLA with 0.5% Eosin + Sodium Bicarbonate Table 8 Coating + Lurol Oil Coating
  • Photoactivatable fibers comprising polypropylene compounded with Eosin Fluorescence Fiber Composition Emission 8 Polypropylene with 0.5% Eosin + Lurol Oil Coating Table 10 9 Polypropylene with 0.5% Eosin + 1% Urea Peroxide Table 11 Coating + Lurol Oil Coating 10 Polypropylene with 0.5% Eosin + Sodium Table 12 Bicarbonate Coating + Lurol Oil Coating 11 Polypropylene with 0.5% Eosin + 10 g/L Eosin Y Table 13 Coating + Lurol Oil Coating
  • Photoactivatable fibers comprising polybutylene terephthalate (PBT) compounded with Eosin Fluorescence Fiber Composition Emission 16 Virgin PBT + Lurol Oil Coating Table 20 17 PBT with 1% Eosin + Lurol Oil Coating Table 21 18 PBT with 1% Eosin + 1% Urea Peroxide Table 22 Coating + Lurol Oil Coating 19 PBT with 1% Eosin + Sodium Bicarbonate Table 23 Coating + Lurol Oil Coating 20 PBT with 1% Eosin + 10 g/L Eosin Y Coating + Table 24 Lurol Oil Coating
  • PBT polybutylene terephthalate
  • Photoactivatable fibers comprising poly(methyl methacrylate) (PMMA) compounded with Eosin Fluorescence Fiber Composition Emission 21 PMMA with 1% Eosin + Lurol Oil Coating Table 26 22 PMMA with 1% Eosin + 1% Urea Peroxide Table 27 Coating + Lurol Oil Coating 23 PrMMA with 1% Eosin + Sodium Bicarbonate Table 28 Coating + Lurol Oil Coating 24 PMMA with 1% Eosin + 10 g/L Eosin Y Table 29 Coating + Lurol Oil Coating
  • the influence of the polymer on the fluorescence emitted by the fibers was measured and compared between the various fibers prepared. The results are presented in FIG. 2D .
  • the data shows that fibers made from polyethylene and PBT fluoresce the most.
  • the purpose of this experiment was to determine whether the polymer has an effect on the leaching of the photoactivatable agent out of the photoactivatable fibers. Leaching was measured by placing 0.1 g of fiber in 10 ml of water for 1 day following which the water was assessed for the presence of photoactivatable agent.
  • FIG. 3 shows the leaching of Eosin out of the photoactivatable fibers as defined in Example 3. The detection limit for samples in FIG. 4 was 0.0095 ⁇ g/ml.
  • Table 34 outlines the data obtained during this experiment. The data presented in Table 34 and illustrated in FIG. 3 demonstrates that photoactivatable fibers made from polyethylene and photoactivatable fibers made from PBT present the least leaching of Eosin amongst the polymers tested. The data also show that compounding the photoactivatable agent with the polymer of the fiber leads to substantially no leaching of the photoactivatable agent out of the photoactivatable fiber.
  • the fluorescence and the energy produced by the photoactivatable fiber increases in a non-linear fashion.
  • nylon fibers the effect is seen in the first five minutes.
  • the fluorescence and energy are 12.95 mW/cm 2 for fluorescence and 1.90 J/cm 2 for energy. After five minutes, it was observed that the fluorescence and the energy were similar.
  • PBT fibers decreasing the lamp height increases both fluorescence and energy.
  • photobleaching occurs more rapidly.
  • PLA fibers decreasing the lamp height increases fluorescence at first. Photobleaching occurs at a rate such that after 7 minutes the fluorescence is lower when the lamp is closer.
  • the purpose of this experiment was to determine if adding more than one layer of photoactivatable agents onto the polymeric fibers affect the emission of fluorescence.
  • the following photoactivatable fibers were prepared.
  • the polypropylene polymer was compounded with the photoactivatable agent (Eosin Y:fluorescein) at around 0.8-1.0% w/w and the polymer was then hardened and cut into small pieces.
  • This polymer was processed into the hopper and it was extruded into a fiber at specific micron sizes ( FIG. 6A : 31 microns) ( FIG. 6B : 93 microns).
  • the amount of fluorophore is determinant for overall fluorescence of the photoactivatable fibers. As the layer level increases the overall fluorescence also increases. The increase is not linear, and doubling the fiber content does not double the fluorescence. It is clear however that 6 layers out preforms both 4 and 2 layers of the same material.
  • a solution of Eosin Y in water was prepared at a concentration of 0.1 g/L, and two polypropylene fibers were dipped in the solution to dope them with chromophore. They were then examined for their fluorescence as seen on DAY 1 to determine how well they retain their fluorescence over time as well as if dipped in water how much chromophore is retained. From this experiment, it can be seen that the tips of the fibers retain fluorescence after 3 days.
  • FIGS. 8A and 8B show the fluorescence emission under blue lamp after one day wherein the fibers were not emerged in water.
  • FIGS. 8C and 8D show the fluorescence emission under blue lamp after three days wherein the fibers were not emerged in water.
  • FIGS. 8E and 8F show the fluorescence emission under blue lamp after three days emerged in water.
  • Eosin Y 300 g/L, 200 g/L, 100 g/L, 50 g/L, 10 g/L, 1 g/L, or 0.1 g/L
  • the fibers were taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively.
  • the 300-100 g/L Eosin Y solutions showed little fluorescence, while the 50 g/L Eosin Y solution showed fluorescence. A significant increase in fluorescence was observed when the 10 g/L Eosin Y solution was used.
  • Dental fibers were dipped into solutions of fluorescein (50 g/L, 10 g/L, 1 g/L, 0.1 g/L) for 10 seconds. The fibers were then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively. The 50 g/L fluorescein solution showed fluorescence.
  • Dental fibers were dipped into solutions of fluorescein:Eosin Y 1:1 (50 g/L, 10 g/L, 1 g/L, 0.1 g/L total chromophore) solution for 10 seconds again. The fibers were then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively.
  • the 50 g/L fluorescein:Eosin Y 1:1 solution showed little fluorescence. A significant increase in fluorescence was observed when the 10 g/L fluorescein:Eosin Y 1:1 solution was used.
  • FIGS. 9A-9P illustrate pictures of the fluorescence emission under blue lamp of fibers dipped in a solution of photoactivatable agents, i.e., commercial dental fibers in Eosin Y 50 g/L ( FIGS. 9A-9B ); commercial dental fibers in Eosin Y 0.1 g/L ( FIGS. 9C-9D ); commercial dental fibers in fluorescein 50 g/L ( FIGS. 9E-19F ), commercial dental fibers in fluorescein 0.1 g/L ( FIGS. 9G-9H ), commercial dental fibers in fluorescein:Eosin Y 50 g/L ( FIG.
  • FIGS. 9I-9J commercial dental fibers in fluorescein:Eosin Y 0.1 g/L ( FIGS. 9K-9L ), polypropylene fibers in fluorescein 50 g/L ( FIGS. 9M-9N ), polypropylene fibers in fluorescein 0.1 g/L ( FIGS. 9O-9P ).
  • Polypropylene fibers were dipped in solutions of fluorescein (50 g/L, 10 g/L, 1 g/L, 0.1 g/L total chromophore) for 10 seconds, then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively.
  • the 50 g/L fluorescein solution showed little fluorescence. An increase in fluorescence was observed when the 10 g/L fluorescein solution was used.
  • the polypropylene fiber used in the preparation of the photoactivatable fabric was acquired from Midwest Filtration (West Chester Township, Ohio, U.S.).
  • the fabric tested was composed of polypropylene at densities ranging from 0.45 oz/yd 2 to 2.50 oz/yd 2 . It was observed that the polypropylene fabric at a density of 2.00 oz/yd 2 absorbs a significant amount of chromophore, while blocking less light than higher thicknesses (data not shown).
  • a piece of the fabric was dipped in a small chromophore bath without Lurol oil PP-3771 while another piece of the fabric was dipped in a small chromophore bath comprising Lurol oil PP-3771. The dipped fabrics were then roll dried and heated in an oven.
  • the process for the preparation of photoactivatable fabric is illustrated in FIG. 10 .
  • the article of manufacture is a suit made of a fabric comprising fibers ( FIG. 11A ).
  • the fibers entering the composition of the fabric may be made of a virgin polymer, that is to say a polymer that does not comprise photoactivatable agent.
  • the fibers entering into the composition of the fabric may be made of photoactivatable fibers which comprise photoactivatable agents.
  • the fabric or the article of manufacture made with such fabric may be coated, dipped or sprayed with a photoactivatable agent composition so as to deposit photoactivatable agents onto the fabric and into the interstices created between the fibers of the fabric.
  • a composition of lubricant may also be laid onto the fabric so as to facilitate the insertion of the photoactivatable agents into the interstices created between the fibers of the fabric.
  • the article of manufacture is a suit which is to be worn by a subject in need of phototherapy ( FIG. 11A ).
  • the photoactivatable fibers that are preferred for entering into the fabrication of the suit comprise nylon and polyethylene which comprise one or more photoactivatable agent.
  • the resulting article of manufacture (e.g., a suit-like garment) is then photoactivated under light while being worn by the subject in need of phototherapy.
  • a suit-like garment was prepared by associating two photoactivatable fabrics having the following composition:
  • the juxtaposed photoactivatable fabrics were tailored into the suit-like garment illustrated in FIG. 11B .
  • the two fabrics may be joined, stitched, glued, attached, fused, sewed, or bonded or the like, and thereafter tailored accordingly.
  • Photoactivatable Fiber/Fabric Composition 36 Fabric 1 - polypropylene fibers (blank - no photoactivatable agent) 37 Fabric 2: polypropylene fibers + Eosin Y 38 Fabric 3: polypropylene fibers + Eosin y and fluorescein 39 Fabric 1 + 1 (2 layers) 40 Fabric 2 + 3 (2 layers)
  • the results represented above are from at least two independent experiments for each media.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Textile Engineering (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pathology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Biophysics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Manufacturing & Machinery (AREA)
  • General Chemical & Material Sciences (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Woven Fabrics (AREA)
  • Artificial Filaments (AREA)
  • Nonwoven Fabrics (AREA)
  • Radiation-Therapy Devices (AREA)
  • Laminated Bodies (AREA)
  • Materials For Medical Uses (AREA)

Abstract

In various aspects, the present disclosure relates to fibers and fabric media comprising photoactivatable agents and to fibers and fabric media that are photoactivatable by photoactivation of the photoactivatable agents. In some instances, the fibers and the fabric media have photoactivatable agents present on their surface (e.g., the fiber/fabric is coated or sprayed with the photoactivatable agents or the fiber/fabric is dipped into a composition or a formulation comprising the photoactivatable agent). In other instances, the photoactivatable agents are incorporated into the materials making the fibers (e.g., the photoactivatable agents are mixed/compounded with the materials making the fibers). The photoactivatable fibers of the present disclosure comprise at least one thermoplastic polymer and at least photoactivatable agent that absorbs and emits light between about 400 nm and about 800 nm.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
This application is a national stage filing under 35 U.S.C. § 371 of International Application No. PCT/CA2015/051118, filed on Oct. 30, 2015, which claims the benefit of and priority to U.S. provisional patent application No. 62/073,795; filed Oct. 31, 2014. The entire contents of each of the foregoing applications are hereby incorporated by reference in their entirety. International Application No. PCT/CA2015/051118 was published under PCT Article 21(2) in English.
FIELD OF TECHNOLOGY
The present disclosure generally relates to photoactivatable fibers and fabric media comprising photoactivable agents, to methods of forming such photoactivatable fibers and fabric media, and to potential uses thereof.
BACKGROUND INFORMATION
Phototherapy has been recognized as having a wide range of applications in both the medical and cosmetic fields including use in surgery, therapy and diagnostics. For example, phototherapy has been used to treat cancers and tumors with lessened invasiveness, to disinfect target sites as an antimicrobial treatment, to treat skin conditions and to promote wound healing.
For these applications, phototherapy has typically been achieved using photoactivatable formulations and/or composition comprising photoactivatable agents capable of absorbing and/or emitting light. These photoactivatable formulations and/or compositions have typically been prepared and/or used as liquids or semi-liquids (e.g., gels, pastes, creams and the like). Due to their liquid and/or semi-liquid texture, some of these photoactivatable formulations and/or compositions exhibit leaching of the photoactivating agents out of the formulations and/or compositions. Also, these formulations and/or compositions require a support/surface onto which they can be are applied. Because they tend to spread and/or dilute in contact with fluids, some liquid and semi-liquid photoactivatable formulations and/or compositions require multiple applications onto the surface to achieve the desired effect. Therefore, the present disclosure relates to photoactivatable formulations having features that may present additional advantages over the photoactivatable formulations known to date. Such features may be useful in phototherapy and may contribute to a wider industrial applicability of the photoactivatable formulations.
SUMMARY OF DISCLOSURE
According to various aspects, the present disclosure relates to a photoactivatable fiber comprising: at least one thermoplastic polymer, and at least one photoactivatable agent; wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
According to various aspects, the present disclosure relates to a photoactivatable fabric comprising a plurality of fibers composed of at least one thermoplastic polymer; and at least one photoactivatable agent, wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
According to various aspects, the present disclosure relates to an article of manufacture comprising a photoactivatable fabric, wherein the photoactivatable fabric comprises: a) a plurality of fibers composed of at least one thermoplastic polymer; and b) at least one photoactivatable agent, wherein the at least one photoactivatable agent absorbs and emits light between about 400 nm and about 800 nm.
According to various aspects, the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying a photoactivatable fiber as defined herein onto the subject; and illuminating the photoactivatable fiber with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
According to various aspects, the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying a photoactivatable fabric as defined herein onto the subject; and illuminating the photoactivatable fabric with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
According to various aspects, the present disclosure relates to a method for effecting phototherapy on a subject, the method comprising applying an article of manufacture as defined herein onto the subject; and illuminating the article of manufacture with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent.
According to various aspects, the present disclosure relates to the use of a photoactivatable fiber as defined herein for effecting phototherapy to a subject.
According to various aspects, the present disclosure relates to the use of a photoactivatable fabric as defined herein for effecting phototherapy to a subject.
According to various aspects, the present disclosure relates to the use of an article of manufacture as defined herein for effecting phototherapy to a subject.
According to various aspects, the present disclosure relates to an article of manufacture comprising a first photoactivatable fabric; and a second photoactivatable fabric; wherein the first and second photoactivatable fabrics are associated with one another and comprise at least one photoactivatable agent that absorbs and emits light between about 400 nm and about 800 nm.
BRIEF DESCRIPTION OF FIGURES
FIGS. 1A-1C. FIG. 1A illustrates a schematic representation of an extruder process used in the preparation of the photoactivatable fibers of the present disclosure. FIG. 1B illustrates a picture of a cross-sectional view of fibers prepared by the extrusion process according to one embodiment of the present disclosure (FIG. 1B showing the core of the fibers). FIG. 1C illustrates a picture of a cross-sectional view of fibers prepared by extrusion process according to another embodiment of the present disclosure, wherein the fibers have a sheath and a core.
FIGS. 2A-2D illustrate graphs showing the fluorescence emission over time of a photoactivatable agent present in nylon fibers (FIG. 2A), PBT fibers (FIG. 2B), and PMMA fibers (FIG. 2C). FIG. 2D illustrates a graph comparing the effect of the polymers tested on fluorescence emission over time of the photoactivatable agents.
FIG. 3 illustrates a graph comparing the leaching of Eosin out of the indicated photoactivatable fibers according to one embodiment of the present disclosure.
FIG. 4 illustrates a graph showing the effect of addition of a lubricant to fluorescence emission by Eosin Y in solution.
FIGS. 5A-5B. FIG. 5A illustrates a graph showing the effect of the presence of a lubricant on fluorescence emission of different concentrations of Eosin Y. FIG. 5B illustrates a graph comparing the effect of the presence of a lubricant on fluorescence emission of Eosin Y and on fluorescence emission of fluorescein.
FIGS. 6A-6B. FIG. 6A illustrates a graph comparing the fluorescence emission over time of a photoactivatable polypropylene fiber according to the present disclosure having 2, 4 or 6 layers of a EosinY:fluorescein composition on its surface. FIG. 6B illustrates a graph comparing the fluorescence emission over time of a photoactivatable nylon fiber according to an embodiment of the present disclosure having 2, 4 or 6 layers of a fluorescein composition on its surface.
FIG. 7 illustrates a graph comparing the fluorescence emission of over time of photoactivatable nylon fibers according to one embodiment of the present disclosure having the photoactivatable agent present inside of the photoactivatable nylon fibers (inner) or on the surface (outer).
FIGS. 8A-8F illustrate pictures of the fluorescence emission of photoactivatable polypropylene fibers according to one embodiment of the present disclosure which were dipped in a solution of Eosin Y (0.1 g/L). FIGS. 8A and 8B show the fluorescence emission under blue lamp after one day wherein the fibers were not emerged in water. FIGS. 8C and 8D show the fluorescence emission under blue lamp after three days wherein the fibers were not emerged in water. FIGS. 8E and 8F show the fluorescence emission under blue lamp after three days emerged in water.
FIGS. 9A-9P illustrate pictures of the fluorescence emission under blue lamp of fibers dipped in a solution of photoactivatable agents, i.e., commercial dental fibers in Eosin Y 50 g/L (FIGS. 9A-9B); commercial dental fibers in Eosin Y 0.1 g/L (FIGS. 9C-9D); commercial dental fibers in fluorescein 50 g/L (FIGS. 9E-19F), commercial dental fibers in fluorescein 0.1 g/L (FIGS. 9G-9H), commercial dental fibers in fluorescein:Eosin Y 50 g/L (FIG. 9I-9J), commercial dental fibers in fluorescein:Eosin Y 0.1 g/L (FIGS. 9K-9L), polypropylene fibers in fluorescein 50 g/L (FIGS. 9M-9N), polypropylene fibers in fluorescein 0.1 g/L (FIGS. 9O-9P).
FIG. 10 illustrates a schematic representation of a process for the preparation of photoactivatable fabrics according to one embodiment of the present disclosure.
FIGS. 11A-11B. FIG. 11A illustrates a schematic representation of an article of manufacture, in occurrence a suit-like garment, according to one embodiment of the present disclosure. FIG. 11B illustrates a picture of a suit-like garment prepared with the photoactivatable fabrics according to one embodiment of the present disclosure.
DETAILED DESCRIPTION
In various aspects, the present disclosure relates to fibers and fabric media comprising photoactivatable agents and to fibers and fabric media that are photoactivatable by photoactivation of the photoactivatable agents. In some instances, the fibers and the fabric media have photoactivatable agents present on their surface (e.g., the fiber/fabric is coated or sprayed with the photoactivatable agents or the fiber/fabric is dipped into a composition or a formulation comprising the photoactivatable agent). In other instances, the photoactivatable agents are incorporated into the materials making the fibers (e.g., the photoactivatable agents are mixed/compounded with the materials making the fibers). In some other implementations, the photoactivatable agents are present both on the surface of the fiber/fabric and incorporated/compounded into the materials making the fibers.
In some instances, the fibers are, but not limited to, synthetic fibers, natural fibers, and textile fibers. For example, synthetic fibers may be made from a polymer or a combination of different polymers. In some instances, the polymer is a thermoplastic polymer.
As used herein, the term “fiber” relates to a string or a thread or a filament used as a component of composite materials. Fibers may be used in the manufacture of other materials such as for example, but not limited to, fabrics.
In some instances, the polymer is acrylic, acrylonitrile butadiene styrene (ABS), polybenzimidazole (PBI), polycarbonate, polyether sulfone (PES), polyetherether ketone (PEEK), polyetherimide (PEI), polyethylene (PE), polyphenylene oxide (PPO), polyphenylene sulfide (PPS), polypropylene (PP), polystyrene, polyvinyl chloride (PVC), teflon, polybutylene, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), nylon, polylactic acid (PLA), polymethyl methacrylate polyester, polyurethane, rayons, poly(methyl methacrylate) (PMMA), or from any mixture thereof.
In some other instances, the fibers may be made from glycolic acid, copolymer lactide/glycolide, polyester polymer, copolymer polyglycolic acid/trimethylene carbonate, natural protein fiber, cellulose fiber, polyamide polymer, polymer of polypropylene, polymer of polyethylene, nylon, polymer of polylactic acid, polymer of polybutylene terephthalate, polyester, copolymer polyglycol, polybutylene, polymer of poly methyl methacrylate, or from any mixture thereof.
In some implementations, the fibers of the present disclosure may be coextruded fibers that have two distinct polymers forming the fiber, usually as a core-sheath or side-by-side.
In some implementations, the fibers may be composed of a single strand (mono-filament) or may be composed of a plurality of strands (multi-filaments). The photoactivatable fibers that are multifilament may also be intertwined or braided or twisted (i.e., the multifilaments are intertwined, braided or twisted to form the fibers).
In some implementations, the diameter of the photoactivatable fiber define herein (taken individually, monofilament) varies between about 15 microns and about 500 microns, between about 25 microns and about 500 microns, between about 50 microns and 400 microns, between about 50 microns and about 300 microns, preferably between about 50 microns and about 250 microns, preferably between about 75 microns and about 300 microns, and most preferably between about 75 microns and about 250 microns. In some specific implementations, the diameter of the photoactivatable fibers defined herein is about 15 microns, about 20 microns, about 25 microns, about 50 microns, about 75 microns, about 100 microns, about 125 microns, about 150 microns, about 175 microns, about 200 microns, about 225 microns, about 250 microns, about 250 microns, about 275 microns, about 300 microns, about 325 microns, about 350 microns, about 375 microns, about 400 microns, about 425 microns, about 450 microns, about 475 microns, about 500 microns. In some instances, the diameter of the photoactivatable fibers defined herein (taken individually) is about 31 microns.
In some implementations, the photoactivatable fibers defined herein show a medium to high resistance to mechanical pulling and stretching forces. In some implementations, the photoactivatable fibers defined here are resilient and have the ability to stretch and to reform to their original size and shape.
In some implementations, the photoactivatable fibers have a linear mass density of between about 400 and about 480 Deniers, between about 410 and about 470 Deniers, between about 420 and about 460 Deniers, between about 420 and about 450 Deniers, or about 428 Deniers. As used herein, the term “Denier” refers to a unit of measure for the linear mass density of fibers, is defined as the mass in grams per 9000 meters.
In some implementations, the fibers defined herein maintain their length and degree of flexibility and windability. In other implementation the stretch fibers may be lubricated to wind and unwind without damage being inflicted on the fibers due to the winding and the unwinding process. In some instance, the fibers have a tensile strength that allows the fibers to be stretched so as to reach a minimum diameter at least half, one third, one fourth, one fifth, one sixth, one seventh, one eight, one ninth, or one tenth of the original diameter.
FIG. 1A illustrates is a schematic representation of an example of a process for preparing photoactivatable fibers according to one embodiment of the present disclosure. In this example, an extrusion process is used wherein polymer pellets are melted and extruded and then pulled into a fiber while still hot. During this process a solution of photoactivatable agents in water and oil is sprayed onto the polymer while it is still hot. The fibers are then spun onto a bobbin for storage and ease of use. In some instances, the photoactivatable fibers of the present disclosure are prepared using a TEM co-rotating twin screw extruder.
In some implementations, the photoactivatable agent is a chemical compound which, when exposed to the light is photoexcited and can then transfer its energy to other molecules or emit it as light, such as for example fluorescence. For example, in some instances, the photoactivable agent when photoexcited by the light may transfer its energy to enhance or accelerate light dispersion or to other molecules such as oxidants to release oxygen radicals. Examples of photoactivable agents include, but are not limited to, fluorescent compounds (or stains) (also known as “fluorochromes” or “fluorophores” or “chromophores”). Other dye groups or dyes (biological and histological dyes, food colorings, carotenoids, and other dyes) can also be used. Suitable photoactivatable agent can be those that are Generally Regarded As Safe (GRAS).
In certain implementations, the photoactivatable fibers of the present disclosure comprise a first photoactivatable agent. In some implementations, the first photoactivatable agent absorbs at a wavelength in the range of the visible spectrum, such as at a wavelength of about 380 nm to about 800 nm, about 380 nm to about 700, about 400 nm to about 800, or about 380 nm to about 600 nm. In other embodiments, the first photoactivating agent absorbs at a wavelength of about 200 nm to about 800 nm, of about 200 nm to about 700 nm, of about 200 nm to about 600 nm or of about 200 nm to about 500 nm. In one embodiment, the first photoactivatable agent absorbs at a wavelength of about 200 nm to about 600 nm. In some embodiments, the first photoactivatable agent absorbs light at a wavelength of about 200 nm to about 300 nm, of about 250 nm to about 350 nm, of about 300 nm to about 400 nm, of about 350 nm to about 450 nm, of about 400 nm to about 500 nm, of about 450 nm to about 650 nm, of about 600 nm to about 700 nm, of about 650 nm to about 750 nm or of about 700 nm to about 800 nm.
In some implementations, the photoactivatable agents emit light within the range of about 400 nm and about 800 nm.
The photoactivatable fibers disclosed herein may include at least one additional photoactivatable agent. Combining photoactivatable agents may increase photo-absorption by the combined dye molecules and enhance absorption and photo-biomodulation selectivity. Thus, in certain embodiments, the photoactivatable fibers of the disclosure include more than one photoactivatable agent.
In the implementations wherein the photoactivatable fibers have the photoactivatable agent on their surface (i.e., the surface of the fibers that is in contact with the surrounding environment of the fiber), such photoactivatable fibers may be prepared by being dipped into a photoactivatable agent composition comprising one or more photoactivatable agents and a carrier material such as, but not limited to, water.
In other implementations wherein the photoactivatable fibers have the photoactivatable agent on their surface (i.e., the surface of the fibers that is in contact with the surrounding environment of the fiber), such photoactivatable fibers may be prepared by being sprayed with a photoactivatable agent composition comprising one or more photoactivatable agents and a carrier material.
In some specific examples, the photoactivatable agent composition has a consistency that allows the fibers to be dipped into the composition. In some specific examples, the photoactivatable agent composition is in a liquid or semi-liquid form.
The carrier material may be any liquid or semi liquid material that is compatible with the photoactivatable agent that is any material that does not affect the photoactive properties of the photoactivatable agent, such as, for example, water. In some other specific examples, the photoactivatable agent composition has a consistency that allows the photoactivatable agent composition to be sprayed onto the fibers.
In the implementations wherein the photoactivatable fibers have the photoactivatable agent incorporated into the fibers, the photoactivatable fibers are prepared by incorporating the photoactivatable agent into the fiber composition. In some examples, the photoactivatable fibers are prepared by extrusion. In some specific implementations, the photoactivatable fibers are prepared by a process which uses spinning. The spinning may be wet, dry, dry jet-wet, melt, gel, or electrospinning. The polymer being spun may be converted into a fluid state. If the polymer is a thermoplastic then it may be melted, otherwise it may be dissolved in a solvent or may be chemically treated to form soluble or thermoplastic derivatives. The molten polymer is then forced through the spinneret, and then it cools to a rubbery state, and then a solidified state. If a polymer solution is used, then the solvent is removed after being forced through the spinneret. A composition of the photoactivatable agent may be added to the polymer in the fluid state or to the melted polymer or to the polymer dissolved into a solvent. Melt spinning may be used for polymers that can be melted. The polymer having the photoactivatable agents dispersed therein solidifies by cooling after being extruded from the spinneret.
The photoactivatable agent may be uniformly or a non-uniformly distributed within the photoactivatable fibers. When the photoactivatable ingredient is uniformly distributed in the photoactivatable fibers, the concentration of photoactivatable agent in the photoactivatable fibers is steady as the photoactivatable fibers disintegrate, whereas when the photoactivatable agent is not uniformly distributed within the photoactivatable fibers, the concentration of the photoactivatable agent in the photoactivatable fibers varies as the photoactivatable fibers disintegrate.
The concentration of the photoactivatable agent to be used may be selected based on the desired intensity and duration of the photoactivity to be emitted from the photoactivatable fibers, and on the desired phototherapeutic, medical or cosmetic effect. For example, some dyes such as xanthene dyes reach a ‘saturation concentration’ after which further increases in concentration do not provide substantially higher emitted fluorescence. Further increasing the photoactivatable agent concentration above the saturation concentration can reduce the amount of activating light passing through the photoactivatable fibers. Therefore, if more fluorescence is required for a certain application than activating light, a high concentration of photoactivatable agent can be used. However, if a balance is required between the emitted fluorescence and the activating light, a concentration close to or lower than the saturation concentration can be chosen.
Suitable photoactivatable agent that may be used in the photoactivatable fibers of the present disclosure include, but are not limited to the following:
Chlorophyll dyes—chlorophyll dyes include but are not limited to chlorophyll a; chlorophyll b; chlorophyllin; bacteriochlorophyll a; bacteriochlorophyll b; bacteriochlorophyll c; bacteriochlorophyll d; protochlorophyll; protochlorophyll a; amphiphilic chlorophyll derivative 1; and amphiphilic chlorophyll derivative 2.
Xanthene derivatives—xanthene dyes include but are not limited to eosin, eosin B (4′,5′-dibromo, 2′,7′-dinitr-o-fluorescein, dianion); eosin Y; eosin Y (2′,4′,5′,7′-tetrabromo-fluorescein, dianion); eosin (2′,4′,5′,7′-tetrabromo-fluorescein, dianion); eosin (2′,4′,5′,7′-tetrabromo-fluorescein, dianion) methyl ester; eosin (2′,4′,5′,7′-tetrabromo-fluorescein, monoanion) p-isopropylbenzyl ester; eosin derivative (2′,7′-dibromo-fluorescein, dianion); eosin derivative (4′,5′-dibromo-fluorescein, dianion); eosin derivative (2′,7′-dichloro-fluorescein, dianion); eosin derivative (4′,5′-dichloro-fluorescein, dianion); eosin derivative (2′,7′-diiodo-fluorescein, dianion); eosin derivative (4′,5′-diiodo-fluorescein, dianion); eosin derivative (tribromo-fluorescein, dianion); eosin derivative (2′,4′,5′,7′-tetrachlor-o-fluorescein, dianion); eosin dicetylpyridinium chloride ion pair; erythrosin B (2′,4′,5′,7′-tetraiodo-fluorescein, dianion); erythrosin; erythrosin dianion; erythiosin B; fluorescein; fluorescein dianion; phloxin B (2′,4′,5′,7′-tetrabromo-3,4,5,6-tetrachloro-fluorescein, dianion); phloxin B (tetrachloro-tetrabromo-fluorescein); phloxine B; rose bengal (3,4,5,6-tetrachloro-2′,4′,5′,7′-tetraiodofluorescein, dianion); pyronin G, pyronin J, pyronin Y; Rhodamine dyes such as rhodamines that include, but are not limited to, 4,5-dibromo-rhodamine methyl ester; 4,5-dibromo-rhodamine n-butyl ester; rhodamine 101 methyl ester; rhodamine 123; rhodamine 6G; rhodamine 6G hexyl ester; tetrabromo-rhodamine 123; and tetramethyl-rhodamine ethyl ester.
Methylene blue dyes—methylene blue derivatives include, but are not limited to, 1-methyl methylene blue; 1,9-dimethyl methylene blue; methylene blue; methylene blue (16 μM); methylene blue (14 μM); methylene violet; bromomethylene violet; 4-iodomethylene violet; 1,9-dimethyl-3-dimethyl-amino-7-diethyl-a-mino-phenothiazine; and 1,9-dimethyl-3-diethylamino-7-dibutyl-amino-phenot-hiazine.
Azo dyes—azo (or diazo-) dyes include but are not limited to methyl violet, neutral red, para red (pigment red 1), amaranth (Azorubine S), Carmoisine (azorubine, food red 3, acid red 14), allura red AC (FD&C 40), tartrazine (FD&C Yellow 5), orange G (acid orange 10), Ponceau 4R (food red 7), methyl red (acid red 2), and murexide-ammonium purpurate.
In some aspects of the disclosure, the one or more photoactivatable agents of the photoactivatable fibers disclosed herein can be independently selected from any of Acid black 1, Acid blue 22, Acid blue 93, Acid fuchsin, Acid green, Acid green 1, Acid green 5, Acid magenta, Acid orange 10, Acid red 26, Acid red 29, Acid red 44, Acid red 51, Acid red 66, Acid red 87, Acid red 91, Acid red 92, Acid red 94, Acid red 101, Acid red 103, Acid roseine, Acid rubin, Acid violet 19, Acid yellow 1, Acid yellow 9, Acid yellow 23, Acid yellow 24, Acid yellow 36, Acid yellow 73, Acid yellow S, Acridine orange, Acriflavine, Alcian blue, Alcian yellow, Alcohol soluble eosin, Alizarin, Alizarin blue 2RC, Alizarin carmine, Alizarin cyanin BBS, Alizarol cyanin R, Alizarin red S, Alizarin purpurin, Aluminon, Amido black 10B, Amidoschwarz, Aniline blue WS, Anthracene blue SWR, Auramine O, Azocannine B, Azocarmine G, Azoic diazo 5, Azoic diazo 48, Azure A, Azure B, Azure C, Basic blue 8, Basic blue 9, Basic blue 12, Basic blue 15, Basic blue 17, Basic blue 20, Basic blue 26, Basic brown 1, Basic fuchsin, Basic green 4, Basic orange 14, Basic red 2, Basic red 5, Basic red 9, Basic violet 2, Basic violet 3, Basic violet 4, Basic violet 10, Basic violet 14, Basic yellow 1, Basic yellow 2, Biebrich scarlet, Bismarck brown Y, Brilliant crystal scarlet 6R, Calcium red, Carmine, Carminic acid, Celestine blue B, China blue, Cochineal, Coelestine blue, Chrome violet CG, Chromotrope 2R, Chromoxane cyanin R, Congo corinth, Congo red, Cotton blue, Cotton red, Croceine scarlet, Crocin, Crystal ponceau 6R, Crystal violet, Dahlia, Diamond green B, Direct blue 14, Direct blue 58, Direct red, Direct red 10, Direct red 28, Direct red 80, Direct yellow 7, Eosin B, Eosin Bluish, Eosin, Eosin Y, Eosin yellowish, Eosinol, Erie garnet B, Eriochrome cyanin R, Erythrosin B, Ethyl eosin, Ethyl green, Ethyl violet, Evans blue, Fast blue B, Fast green FCF, Fast red B, Fast yellow, Fluorescein, Food green 3, Gallein, Gallamine blue, Gallocyanin, Gentian violet, Haematein, Haematine, Haematoxylin, Helio fast rubin BBL, Helvetia blue, Hematein, Hematine, Hematoxylin, Hoffman's violet, Imperial red, Indocyanin Green, Ingrain blue, Ingrain blue 1, Ingrain yellow 1, INT, Kermes, Kermesic acid, Kernechtrot, Lac, Laccaic acid, Lauth's violet, Light green, Lissamine green SF, Luxol fast blue, Magenta 0, Magenta I, Magenta II, Magenta III, Malachite green, Manchester brown, Martius yellow, Merbromin, Mercurochrome, Metanil yellow, Methylene azure A, Methylene azure B, Methylene azure C, Methylene blue, Methyl blue, Methyl green, Methyl violet, Methyl violet 2B, Methyl violet 10B, Mordant blue 3, Mordant blue 10, Mordant blue 14, Mordant blue 23, Mordant blue 32, Mordant blue 45, Mordant red 3, Mordant red 11, Mordant violet 25, Mordant violet 39 Naphthol blue black, Naphthol green B, Naphthol yellow S, Natural black 1, Natural green 3(chlorophyllin), Natural red, Natural red 3, Natural red 4, Natural red 8, Natural red 16, Natural red 25, Natural red 28, Natural yellow 6, NBT, Neutral red, New fuchsin, Niagara blue 3B, Night blue, Nile blue, Nile blue A, Nile blue oxazone, Nile blue sulphate, Nile red, Nitro BT, Nitro blue tetrazolium, Nuclear fast red, Oil red O, Orange G, Orcein, Pararosanilin, Phloxine B, Picric acid, Ponceau 2R, Ponceau 6R, Ponceau B, Ponceau de Xylidine, Ponceau S, Primula, Purpurin, Pyronin B, phycobilins, Phycocyanins, Phycoerythrins. Phycoerythrincyanin (PEC), Phthalocyanines, Pyronin G, Pyronin Y, Quinine, Rhodamine B, Rosanilin, Rose bengal, Saffron, Safranin O, Scarlet R, Scarlet red, Scharlach R, Shellac, Sirius red F3B, Solochrome cyanin R, Soluble blue, Solvent black 3, Solvent blue 38, Solvent red 23, Solvent red 24, Solvent red 27, Solvent red 45, Solvent yellow 94, Spirit soluble eosin, Sudan III, Sudan IV, Sudan black B, Sulfur yellow S, Swiss blue, Tartrazine, Thioflavine S, Thioflavine T, Thionin, Toluidine blue, Toluyline red, Tropaeolin G, Trypaflavine, Trypan blue, Uranin, Victoria blue 4R, Victoria blue B, Victoria green B, Vitamin B, Water blue I, Water soluble eosin, Xylidine ponceau, or Yellowish eosin.
In certain embodiments, the photoactivatable fibers of the present disclosure may include any of the photoactivatable agents listed above, or a combination thereof, so as to provide a synergistic biophotonic effect. For example, the following synergistic combinations of photoactivatable agents may be used: Eosin Y and Fluorescein; Fluorescein and Rose Bengal; Erythrosine in combination with Eosin Y, Rose Bengal or Fluorescein; Phloxine B in combination with one or more of Eosin Y, Rose Bengal, Fluorescein and Erythrosine; Eosin Y, Fluorescein and Rose Bengal.
In some examples, the photoactivatable agent is present in the photoactivatable agent composition at a concentration of about 100 g/L, about 50 g/L, about 10 g/L, about 5 g/L, about 1 g/L or about 0.1 g/L of the total volume. Preferably, the photoactivatable agent is present in the photoactivatable agent composition at a concentration of between about 10 g/L and about 100 g/L. In some instances, the photoactivatable agent is present in the photoactivatable agent composition at a concentration that is lower than 0.1 g/L, for example, the photoactivatable agent is present in the photoactivatable agent composition at a concentration in the milligram/L or in the microgram/L range.
In some embodiments, the photoactivatable fibers of the present disclosure comprise a lubricant. In some instances, the lubricant is coated onto the photoactivatable fibers of the present disclosure. In some instances, the lubricant is treatment oil, such as but not limited to Polyethylene glycol esters (e.g., Lurol Oil™). Without wishing to be bound by theory, the addition of a lubricant to the surface of the fibers improves the retention of the composition of photoactivatable agents onto the fibers. For example, the lubricant improves the hydrophilicity of the polymer so that it increases the absorption of the solution of photoactivatable agent.
In some implementations, there is less than about 15% leaching of the photoactivatable agent out of the photoactivatable fibers of the present disclosure, more preferably less than 10%, more preferably less than 5%, more preferably less than 4%, more preferably less than 3%, more preferably less than 2%, more preferably less than 1%, or even more preferably substantially no leaching of the photoactivatable agent out of the photoactivatable fibers. Leaching of the photoactivatable agent out of the photoactivatable fibers of the present disclosure may be assessed by placing 0.1 g of the photoactivatable fibers in 10 ml of water for 1 day and by then measuring the amount of photoactivatable agent in the water.
In some implementations, the photoactivatable fibers as defined herein may be woven into a fabric material resulting in a photoactivatable fabric comprising a plurality of photoactivatable fibers. In some implementations, the photoactivatable fabric comprising the photoactivatable fibers exhibits substantially no leaching of the photoactivatable agent.
As used herein, the term “fabric” relates to a woven material composed of a network of fibers or to a non-woven (e.g., spunbound) material composed of fibers. Weaving is a method of textile production in which two distinct sets of yarns or threads are interlaced at right angles to form a fabric or cloth. Similar methods are knitting, felting, and braiding or plaiting. Non-woven fabrics are broadly defined as sheet or web structures bonded together by entangling fiber or filaments mechanically, thermally or chemically. They are flat or tufted porous sheets that are made directly from separate fibers, molten plastic or plastic film. They are not made by weaving or knitting and do not require converting the fibers to yarn.
In some examples, the fabric material may be used in the fabrication of an article of manufacture such as, but not limited to, a garment, an article of clothing, a wound dressing, a towel, bedding, and the like. In some implementation the garment may be a shirt, pants, glove, mask, socks, or the like. In some instances, the photoactivatable fibers of the present disclosure are woven into a fabric material is a suit or a suit-like garment.
In the implementations wherein the photoactivatable agents are compounded with the polymer of the fibers, the fabric made from such fibers is also photoactivatable. Whereas in the implementations wherein the photoactivatable agents are not compounded with the polymer of the fibers, the fabric made from such fibers may be coated or dipped or sprayed with a photoactivatable agent composition to render the fabric photoactivatable.
In some other examples, the photoactivatable fabric may be a nonwoven photoactivatable fabric such as but not limited to a spunbound fabric. Spunbond fabrics may be produced by depositing extruded, spun filaments onto a collecting belt in a uniform random manner followed by bonding the fibers. The fibers may be separated during the web laying process by air jets or electrostatic charges. The collecting surface is usually perforated to prevent the air stream from deflecting and carrying the fibers in an uncontrolled manner. Bonding imparts strength and integrity to the web by applying heated rolls or hot needles to partially melt the polymer and fuse the fibers together. In general, high molecular weight and broad molecular weight distribution polymers such as, but not limited to, polypropylene, polyester, polyethylene, polyethylene terephthalate, nylon, polyurethane, and rayons may be used in the manufacture of spunbound fabrics. In some instances, spunbound fabrics may be composed of a mixture of polymers. A lower melting polymer can function as the binder which may be a separate fiber interspersed with higher melting fibers, or two polymers may be combined into a single fiber type. In the latter case the so-called bi-component fibers possess a lower melting component, which acts as a sheath covering over a higher melting core. Bicomponent fibers may also spun by extrusion of two adjacent polymers.
In some instances, spunbonding may combine fiber spinning with web formation by placing the bonding device in line with spinning. In some arrangements the web may be bonded in a separate step. The spinning process may be similar to the production of continuous filament yarns and may utilize similar extruder conditions for a given polymer. Fibers are formed as the molten polymer exits the spinnerets and is quenched by cool air. The objective of the process is to produce a wide web and, therefore, many spinnerets are placed side by side to generate sufficient fibers across the total width.
Before deposition on a moving belt or screen, the output of a spinneret usually includes a plurality of individual filaments which must be attenuated to orient molecular chains within the fibers to increase fiber strength and decrease extensibility. This is accomplished by rapidly stretching the plastic fibers immediately after exiting the spinneret. In practice the fibers are accelerated either mechanically or pneumatically. The web is formed by the pneumatic deposition of the filament bundles onto the moving belt. A pneumatic gun uses high-pressure air to move the filaments through a constricted area of lower pressure, but higher velocity as in a venturi tube. In order for the web to achieve maximum uniformity and cover, individual filaments are separated before reaching the belt. This is accomplished by inducing an electrostatic charge onto the bundle while under tension and before deposition. The charge may be induced triboelectrically or by applying a high voltage charge. The belt is usually made of an electrically grounded conductive wire. Upon deposition, the belt discharges the filaments. Webs produced by spinning linearly arranged filaments through a so-called slot die eliminating the need for such bundle separating devices.
Many methods can be used to bond the fibers in the spun web. These include mechanical needling, thermal bonding, and chemical bonding. The last two may bond large regions (area bonding) or small regions (point bonding) of the web by fusion or adhesion of fibers. Point bonding results in the fusion of fibers at points, with fibers between the point bonds remaining relatively free. Other methods used with staple fiber webs, but not routinely with continuous filament webs include stitch bonding, ultrasonic fusing, and hydraulic entanglement.
The photoactivatable fabrics of the present disclosure preferably have a thickness that allows light to reach the photoactivatable agents embedded in the fibers of the fabric and for the light emitted by the photoactivatable agents to exit the fabric.
In some embodiments, the photoactivatable fibers and the photoactivatable fabrics of the present disclosure may have cosmetic and/or medical benefits.
In some implementations of these embodiments, the photoactivatable fibers and the photoactivatable fabrics may be used to promote prevention and/or treatment of a tissue or an organ and/or to treat a tissue or an organ of a subject in need of phototherapy.
In some instances, the photoactivatable fibers and/fabrics of the present disclosure may be used to promote treatment of a skin disorder such as acne, eczema, dermatitis or psoriasis, promote tissue repair, and modulate inflammation, modulate collagen synthesis, reduce or avoid scarring, for cosmesis, or promote wound healing. They can be used to treat acute inflammation. Acute inflammation can present itself as pain, heat, redness, swelling and loss of function, and includes inflammatory responses such as those seen in allergic reactions such as those to insect bites e.g.; mosquito, bees, wasps, poison ivy, or post-ablative treatment.
In certain instance, the photoactivatable fibers and/fabrics of the present disclosure may provide treatment of a skin disorder, preventing or treating scarring, and/or accelerating wound healing and/or tissue repair.
In certain embodiments, the photoactivatable fibers or fabrics may be used to promote wound healing. In this case, the photoactivatable fibers or fabrics may be applied at wound site as deemed appropriate by the physician or other health care providers. In certain embodiments, the photoactivatable fibers or fabrics may be used following wound closure to optimize scar revision. In this case, the photoactivatable fibers or fabrics may be applied at regular intervals such as once a week, or at an interval deemed appropriate by the physician or other health care providers.
In certain embodiments, the photoactivatable fibers or fabrics may be used following acne treatment to maintain the condition of the treated skin. In this case, the photoactivatable fibers or fabrics may be applied at regular intervals such as once a week, or at an interval deemed appropriate by the physician or other health care providers.
In certain embodiments, the photoactivatable fibers or fabrics may be used following ablative skin treatment to maintain the condition of the treated skin.
The photoactivatable fibers or fabrics of the present disclosure may be used to treat skin disorders that include, but are not limited to, erythema, telangiectasia, actinic telangiectasia, basal cell carcinoma, contact dermatitis, dermatofibrosarcoma protuberans, genital warts, hidradenitis suppurativa, melanoma, merkel cell carcinoma, nummular dermatitis, molloscum contagiosum, psoriasis, psoriatic arthritis, rosacea, scabies, scalp psoriasis, sebaceous carcinoma, squamous cell carcinoma, seborrheic dermatitis, seborrheic keratosis, shingles, tinea versicolor, warts, skin cancer, pemphigus, sunburn, dermatitis, eczema, rashes, impetigo, lichen simplex chronicus, rhinophyma, perioral dermatitis, pseudofolliculitis barbae, drug eruptions, erythema multiforme, erythema nodosum, granuloma annulare, actinic keratosis, purpura, alopecia areata, aphthous stomatitis, dry skin, chapping, xerosis, fungal infections, herpes simplex, intertrigo, keloids, keratoses, milia, moluscum contagiosum, pityriasis rosea, pruritus, urticaria, and vascular tumors and malformations. Dermatitis includes contact dermatitis, atopic dermatitis, seborrheic dermatitis, nummular dermatitis, generalized exfoliative dermatitis, and statis dermatitis. Skin cancers include melanoma, basal cell carcinoma, and squamous cell carcinoma.
The photoactivatable fibers or fabrics of the present disclosure may be used to treat acne. As used herein, “acne” means a disorder of the skin caused by inflammation of skin glands or hair follicles. The photoactivatable fibers or fabrics of the disclosure can be used to treat acne at early pre-emergent stages or later stages where lesions from acne are visible. Mild, moderate and severe acne can be treated with embodiments of photoactivatable fibers or fabrics. Early pre-emergent stages of acne usually begin with an excessive secretion of sebum or dermal oil from the sebaceous glands located in the pilosebaceous apparatus. Sebum reaches the skin surface through the duct of the hair follicle. The presence of excessive amounts of sebum in the duct and on the skin tends to obstruct or stagnate the normal flow of sebum from the follicular duct, thus producing a thickening and solidification of the sebum to create a solid plug known as a comedone. In the normal sequence of developing acne, hyperkeratinazation of the follicular opening is stimulated, thus completing blocking of the duct. The usual results are papules, pustules, or cysts, often contaminated with bacteria, which cause secondary infections. Acne is characterized particularly by the presence of comedones, inflammatory papules, or cysts. The appearance of acne may range from slight skin irritation to pitting and even the development of disfiguring scars. Accordingly, the photoactivatable fibers or fabrics of the present disclosure can be used to treat one or more of skin irritation, pitting, development of scars, comedones, inflammatory papules, cysts, hyperkeratinazation, and thickening and hardening of sebum associated with acne.
Some skin disorders present various symptoms including redness, flushing, burning, scaling, pimples, papules, pustules, comedones, macules, nodules, vesicles, blisters, telangiectasia, spider veins, sores, surface irritations or pain, itching, inflammation, red, purple, or blue patches or discolorations, moles, and/or tumors.
The photoactivatable fibers or fabrics of the present disclosure may be used to treat various types of acne. Some types of acne include, for example, acne vulgaris, cystic acne, acne atrophica, bromide acne, chlorine acne, acne conglobata, acne cosmetica, acne detergicans, epidemic acne, acne estivalis, acne fulminans, halogen acne, acne indurata, iodide acne, acne keloid, acne mechanica, acne papulosa, pomade acne, premenstral acne, acne pustulosa, acne scorbutica, acne scrofulosorum, acne urticata, acne varioliformis, acne venenata, propionic acne, acne excoriee, gram negative acne, steroid acne, and nodulocystic acne.
In certain embodiments, the photoactivatable fibers or fabrics of the present disclosure are used in conjunction with systemic or topical antibiotic treatment. For example, antibiotics used to treat acne include tetracycline, erythromycin, minocycline, doxycycline. In some implementations, the article of manufacture being composed of the photoactivatable fabric of the present disclosure may have an anti-infective effect, for example when used in the treatment of a wound to prevent infection and/or re-infection of the wound by bacteria or by other infective agents.
The photoactivatable fibers or fabrics of the present disclosure may be used to treat wounds, promote wound healing, promote tissue repair and/or prevent or reduce cosmesis including improvement of motor function (e.g. movement of joints). Wounds that may be treated by the photoactivatable fibers and fabrics of the present disclosure include, for example, injuries to the skin and subcutaneous tissue initiated in different ways (e.g., pressure ulcers from extended bed rest, wounds induced by trauma or surgery, burns, ulcers linked to diabetes or venous insufficiency) and with varying characteristics. In certain embodiments, the present disclosure provides photoactivatable fibers or fabrics for treating and/or promoting the healing of, for example, burns, incisions, excisions, lesions, lacerations, abrasions, puncture or penetrating wounds, surgical wounds, contusions, hematomas, crushing injuries, amputations, sores and ulcers.
In some embodiments, the photoactivatable fibers and fabrics of the present disclosure may be used in a method for effecting phototherapy on a subject, such as on a tissue and/or an organ of the subject. Such method comprises the step of applying a photoactivatable fibers and fabric as defined herein onto the subject or onto the tissue or the organ in need of phototherapy and the step of illuminating the photoactivatable fiber and fabric with light having a wavelength that overlaps with that overlaps with an absorption spectrum of the photoactivatable agent.
In certain instances, the photoactivatable fibers and fabrics of the present disclosure may be used in phototherapy and/or in biophotonic therapy. In certain instances, the photoactivatable fibers and fabrics of the present disclosure may be used as biophotonic medical devices.
In certain instances, the photoactivatable fibers and fabrics of the present disclosure may be used in the manufacture of medical devices such as suture materials, stents, catheter, balloons, wound dressing or the like. In some other embodiments, the photoactivatable fibers may be used in the fabrication of dental care devices such as in the fabrication of toothbrush, dental floss, braces and the like.
The methods of the present disclosure comprise applying a photoactivatable fiber or photoactivatale fabric of the present disclosure to a tissue or organ in need of phototherapy and illuminating the photoactivatable fiber or photoactivatale fabric with light having a wavelength that overlaps with an absorption spectrum of the photoactivatable agent(s) present in the photoactivatable fiber or photoactivatable fabric to induce emission of the photoactivatable agent(s).
In the methods of the present disclosure, any source of actinic light can be used. Any type of halogen, LED or plasma arc lamp, or laser may be suitable. The primary characteristic of suitable sources of actinic light will be that they emit light in a wavelength (or wavelengths) appropriate for activating the one or more photoactivatable agent present in the composition. In one embodiment, an argon laser is used. In another embodiment, a potassium-titanyl phosphate (KTP) laser (e.g. a GreenLight™ laser) is used. In yet another embodiment, a LED lamp such as a photocuring device is the source of the actinic light. In yet another embodiment, the source of the actinic light is a source of light having a wavelength between about 200 to 800 nm. In another embodiment, the source of the actinic light is a source of visible light having a wavelength between about 400 and 600 nm. In another embodiment, the source of the actinic light is a source of visible light having a wavelength between about 400 and 700 nm. In yet another embodiment, the source of the actinic light is blue light. In yet another embodiment, the source of the actinic light is red light. In yet another embodiment, the source of the actinic light is green light. Furthermore, the source of actinic light should have a suitable power density. Suitable power density for non-collimated light sources (LED, halogen or plasma lamps) are in the range from about 0.1 mW/cm2 to about 200 mW/cm2. Suitable power density for laser light sources are in the range from about 0.5 mW/cm2 to about 0.8 mW/cm2.
In some implementations, the light has an energy at the subject's skin surface of between about 0.1 mW/cm2 and about 500 mW/cm2, or 0.1-300 mW/cm2, or 0.1-200 mW/cm2, wherein the energy applied depends at least on the condition being treated, the wavelength of the light, the distance of the skin from the light source and the thickness of the photoactivatable fibers or fabrics. In certain embodiments, the light at the subject's skin is between about 1-40 mW/cm2, or between about 20-60 mW/cm2, or between about 40-80 mW/cm2, or between about 60-100 mW/cm2, or between about 80-120 mW/cm2, or between about 100-140 mW/cm2, or between about 30-180 mW/cm2, or between about 120-160 mW/cm2, or between about 140-180 mW/cm2, or between about 160-200 mW/cm2, or between about 110-240 mW/cm2, or between about 110-150 mW/cm2, or between about 190-240 mW/cm2.
The activation of the photoactivatable agents may take place almost immediately on illumination (femto- or pico seconds). A prolonged exposure period may be beneficial to exploit the synergistic effects of the absorbed, reflected and reemitted light of the photoactivatable fibers and fabrics of the present disclosure and its interaction with the tissue being treated. In one embodiment, the time of exposure of photoactivatable fibers or fabrics to actinic light is a period between 0.01 minutes and 90 minutes. In another embodiment, the time of exposure of the photoactivatable fibers or fabrics to actinic light is a period between 1 minute and 5 minutes. In some other embodiments, the photoactivatable fibers or fabrics are illuminated for a period between 1 minute and 3 minutes. In certain embodiments, light is applied for a period of about 1-30 seconds, about 15-45 seconds, about 30-60 seconds, about 0.75-1.5 minutes, about 1-2 minutes, about 1.5-2.5 minutes, about 2-3 minutes, about 2.5-3.5 minutes, about 3-4 minutes, about 3.5-4.5 minutes, about 4-5 minutes, about 5-10 minutes, about 10-15 minutes, about 15-20 minutes, or about 20-30 minutes. The treatment time may range up to about 90 minutes, about 80 minutes, about 70 minutes, about 60 minutes, about 50 minutes, about 40 minutes or about 30 minutes. It will be appreciated that the treatment time can be adjusted in order to maintain a dosage by adjusting the rate of fluence delivered to a treatment area. For example, the delivered fluence may be about 4 to about 60 J/cm2, 4 to about 90 J/cm2, 10 to about 90 J/cm2, about 10 to about 60 J/cm2, about 10 to about 50 J/cm2, about 10 to about 40 J/cm2, about 10 to about 30 J/cm2, about 20 to about 40 J/cm2, about 15 J/cm2 to 25 J/cm2, or about 10 to about 20 J/cm2.
In certain embodiments, the photoactivatable fibers and photoactivatable fabric may be re-illuminated at certain intervals. In yet another embodiment, the source of actinic light is in continuous motion over the treated area for the appropriate time of exposure. In yet another embodiment, the photoactivatable fibers or photoactivatable fabric may be illuminated until the photoactivatable fibers or photoactivatable fabric is at least partially photobleached or fully photobleached.
In certain embodiments, the photoactivatable agents in the photoactivatable fibers or fabrics can be photoexcited by ambient light including from the sun and overhead lighting. In certain embodiments, the photoactivatable agents can be photoactivated by light in the visible range of the electromagnetic spectrum. The light can be emitted by any light source such as sunlight, light bulb, an LED device, electronic display screens such as on a television, computer, telephone, mobile device, flashlights on mobile devices. In the methods of the present disclosure, any source of light can be used. For example, a combination of ambient light and direct sunlight or direct artificial light may be used. Ambient light can include overhead lighting such as LED bulbs, fluorescent bulbs, and indirect sunlight.
In the methods of the present disclosure, the photoactivatable fibers or fabric may be removed from the tissue or organ following application of light. In other embodiments, the photoactivatable fibers or fabric may be left on the tissue or organ for an extended period of time and re-activated with direct or ambient light at appropriate times to treat the condition.
EXAMPLES Example 1 Preparation of Photoactivatable Fibers and Photoactivatable Fabrics
Chromophores were incorporated into fibers made of polymer materials (polymer materials compounded with chromophores). The compounding involved taking a polymer melt and adding the chromophores in their solid form directly to the polymer, and then allowing the melt to cool. This process allowed chromophores to be integrated with the polymer fibers. The polymer fibers were selected from fibers, nonwoven fabrics, tubes and films. The chromophore to polymer ratio was selected so as to be dependent on the chromophore used, for example: for Eosin Y, 20% w/w ratio (in water) was used for the master chromophore batch, for Fluorescein, 5% w/w ratio was used for the master chromophore batch. A pure Eosin Y fiber was made and a 4:1 mixture (by weight (or 1:1 by fiber weight)) of Eosin Y and Fluorescein was made.
Preparation of the Fibers:
Fibers made of polypropylene, of polyethylene, nylon, or of a combination thereof were prepared. Eosin Y or fluorescein or a combination of Eosin Y and fluorescein were used as photoactivatable agents. A cross-sectional view of the fibers prepared using one type of polymer is shown in FIG. 1B. The polyethylene was made into a 50/50 polyethylene core with a polypropylene sheath. A cross-sectional view of these fibers is shown in FIG. 1C.
Fibers having the following composition have been considered:
    • A) Polypropylene polymer and 5% Eosin Y,
    • B) Polypropylene polymer and 10% Eosin Y,
    • C) Polypropylene polymer and 15% Eosin Y,
    • D) Polypropylene polymer and 20% Eosin Y,
    • E) Polypropylene polymer and 5% Eosin Y
    • F) Polypropylene polymer and 10% Fluorescein,
    • G) Polypropylene polymer and 15% Eosin Y;
    • H) Polypropylene polymer and 20% Eosin Y
    • I) Polyethylene polymer and 5% Eosin Y,
    • J) Polyethylene polymer and 10% Eosin Y,
    • K) Polyethylene polymer and 15% Eosin Y,
    • L) Polyethylene polymer and 20% Eosin Y,
    • M) Polyethylene polymer and 5% Fluorescein,
    • N) Nylon and 5% Eosin Y,
    • O) Nylon and 10% Eosin Y,
    • P) Nylon and 15% Eosin Y,
    • Q) Nylon and 20% Eosin Y,
    • R) Nylon and 5% Fluorescein.
Non-Woven Fabric:
Polypropylene fibers were used as non-woven samples. The following fibers were prepared:
    • S) Polypropylene polymer and 0.5 g/L Eosin Y,
    • T) Polypropylene polymer and 0.5 g/L Eosin Y and 0.25 g/L fluorescein.
Example 2 Preparation of Photoactivatable Fibers with Lubricant
Fibers were dipped in a bath of chromophore and lubricant (1:6 oil:water) (i.e., lurol oil) to produce fibers that were colored and that fluoresced. The fibers incorporated two chromophores, both Eosin Y and a fluorescein/Eosin Y mixture (1/4). The polyethylene was made into a 50/50 polyethylene core with a polypropylene sheath.
Fibers having the following composition have been considered:
    • AA) Polymethyl methacrylate (Sheath) with Polypropylene (Core), Eosin Y:Fluorescein 10 g/L each, 150 micron monofilament,
    • BB) Polymethyl methacrylate (Sheath) with Polypropylene (Core), Eosin Y:Fluorescein 20 g/L each, 150 micron monofilament,
    • CC) Polymethyl methacrylate (Sheath) with Polypropylene (Core), Eosin Y:Fluorescein 30 g/L each, 150 micron monofilament,
    • DD) Nylon, Eosin Y:Fluorescein 10 g/L each, 150 micron multifilament,
    • EE) Nylon, Eosin Y:Fluorescein 20 g/L each, 150 micron multifilament,
    • FF) Nylon, Eosin Y: Fluorescein 50 g/L each, 150 micron multifilament,
    • GG) Polypropylene, Eosin Y Chromophore 20%, 2 pounds,
    • HH) Polypropylene, Eosin Y Chromophore 20%, 1 pounds MIXED WITH polypropylene, Fluorescein Chromophore 5%, 1 pounds (1:1 Ratio) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 1 pound AND polypropylene Core blank, Blank, 1 pound,
    • II) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 0.5 pounds MIXED WITH polyethylene Sheath doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio),
    • JJ) Polypropylene Core blank, Blank, 1 pound,
    • KK) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 1 pound AND polypropylene Core doped with, Eosin Y Chromophore 20%, 1 pound,
    • LL) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 0.5 pounds MIXED WITH polyethylene Sheath doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio) AND polypropylene Core doped with, Eosin Y Chromophore 20%, 1 pound,
    • MM) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 0.5 pounds MIXED WITH polyethylene Sheath doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio) AND polypropylene Core doped with, Eosin Y Chromophore 20%, 0.5 pounds MIXED WITH polypropylene Core doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio),
    • NN) Polyethylene Sheath blank, Blank, 1 pound WITH polypropylene Core doped with, Eosin Y Chromophore 20%, 1 pound,
    • OO) Polyethylene Sheath blank, Blank, 1 pound AND polypropylene core doped with, Eosin Y Chromophore 20%, 0.5 pounds MIXED WITH polypropylene core doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio),
    • PP) Polyethylene Sheath doped with, Eosin Y Chromophore 20%, 1 pound AND polypropylene core doped with, Eosin Y Chromophore 20%, 0.5 pound MIXED WITH polypropylene core doped with, Fluorescein Chromophore 5%, 0.5 pounds (1:1 Ratio)
    • QQ) Nylon, Eosin Y Chromophore 20%, 2 pounds,
    • RR) Nylon, Eosin Y Chromophore 20%, 1 pound MIXED WITH Nylon, Fluorescein Chromophore 5%, 1 pound (1:1 Ratio).
Example 3 Fluorescence Emission by Photoactivatable Fibers
The photoactivatable fibers outlined in Tables 1, 5, 9, 14, 19 and 25 were prepared; a composition of photoactivatable agents was sprayed onto some of the fibers. Each of these fibers was assessed for its ability to emit fluorescence following illumination for 5 mins at 5 cm using a Thera™ Lamp. The results are presented in FIG. 2A (nylon fibers), FIG. 2B (PBT fibers) and FIG. 2C (PMMA fibers) and in Tables 2, 3, 4, 6, 7, 8, 10, 11, 12, 13, 15, 16, 17, 18, 20, 21, 22, 23, 24, 26, 27, 28, 29, 30, 31, 32 and 33.
TABLE 1
Photoactivatable fibers comprising
polyethylene compounded with Eosin
Fluorescence
Fiber Composition Emission
1 Polyethylene with 0.5% Eosin + Lurol Oil Coating Table 2
2 Polyethylene with 0.5% Eosin + 1% Urea Peroxide Table 3
Coating + Lurol Oil Coating
3 Polyethylene with 0.5% Eosin + Sodium Table 4
Bicarbonate Coating + Lurol Oil Coating
4 Polyethylene with 0.5% Eosin + 10 g/L Eosin Y
Coating + Lurol Oil Coating
TABLE 2
Fiber 1 - Polyethylene + Eosin Inside, Lurol Oil Outside
Fiber 1 -
Polyethylene + Eosin
Inside, Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 37.73 37.83 37.89 37.91 38.04 38.18 38.28
Fluoresc. 519-760 0.03 0.03 0.03 0.03 0.03 0.03 0.02
total 400-760 37.76779 37.85432 37.9151 37.94457 38.06825 38.2112 38.30258
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.1% 0.1% 0.1%
purple (400)-450  25.7413 25.4023 25.1707 24.9117 24.7605 24.6212 24.4817
Blue 450-500 11.9843 12.4069 12.6914 12.9768 13.2592 13.5382 13.7734
Green 500-570 0.0117 0.0197 0.0307 0.0279 0.0259 0.0267 0.0338
Yellow 570-591 0.0065 0.0067 0.0092 0.0102 0.0093 0.0092 0.0056
Orange 591-610 0.0054 0.0098 0.0088 0.0110 0.0091 0.0096 0.0064
Red 610-760 0.0188 0.0094 0.0047 0.0075 0.0047 0.0068 0.0019
total (400-700) 37.77 37.85 37.92 37.95 38.07 38.21 38.30
Fiber 1 -
Polyethylene + Eosin
Inside, Lurol Oil mW/cm2 at 5 cm
Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 38.36 38.44 38.56 38.61 11.44 99.9%
Fluoresc. 519-760 0.03 0.03 0.02 0.02 0.01 0.1%
total 400-760 38.38788 38.4684 38.58573 38.6291 11.45 100.0%
% fluorescence 0.1% 0.1% 0.1% 0.0% 0.00 0.1%
purple (400)-450  24.3537 24.2225 24.1625 24.0604 7.43 65.0%
Blue 450-500 13.9839 14.1869 14.3716 14.5227 4.00 34.9%
Green 500-570 0.0334 0.0415 0.0349 0.0313 0.01 0.1%
Yellow 570-591 0.0071 0.0108 0.0064 0.0058 0.00 0.0%
Orange 591-610 0.0074 0.0064 0.0072 0.0056 0.00 0.0%
Red 610-760 0.0026 0.0005 0.0035 0.0035 0.00 0.0%
total (400-700) 38.39 38.47 38.59 38.63 11.45 100.0%
TABLE 3
Fiber 2 - with Urea Peroxide in Lurol Oil
Fiber 2 - with Urea mW/cm2 at 5 cm
Peroxide in Lurol Oil 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 44.34 43.56 43.60 43.59 43.53 43.48 43.45
Fluoresc. 519-760 0.03 0.03 0.03 0.03 0.03 0.04 0.03
total 400-760 44.364 43.59121 43.63011 43.62437 43.55596 43.52089 43.48319
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.1% 0.1% 0.1%
purple (400)-450  28.7823 27.7839 27.6486 27.3997 27.1146 26.9311 26.7372
Blue 450-500 15.5221 15.7414 15.9171 16.1574 16.3843 16.5173 16.6797
Green 500-570 0.0376 0.0415 0.0369 0.0431 0.0308 0.0436 0.0389
Yellow 570-591 0.0091 0.0094 0.0112 0.0094 0.0083 0.0111 0.0072
Orange 591-610 0.0076 0.0087 0.0106 0.0103 0.0099 0.0111 0.0107
Red 610-760 0.0055 0.0069 0.0060 0.0049 0.0085 0.0072 0.0101
total (400-700) 44.36 43.59 43.63 43.62 43.56 43.52 43.48
Fiber 2 - with Urea mW/cm2 at 5 cm
Peroxide in Lurol Oil 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 43.47 43.48 43.60 43.69 13.08 99.9%
Fluoresc. 519-760 0.03 0.03 0.04 0.04 0.01 0.1%
total 400-760 43.49531 43.50617 43.63938 43.72855 13.09 100.0%
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.00 0.1%
purple (400)-450  26.5918 26.4659 26.4030 26.3381 8.16 62.3%
Blue 450-500 16.8401 16.9717 17.1625 17.3136 4.92 37.6%
Green 500-570 0.0393 0.0406 0.0504 0.0474 0.01 0.1%
Yellow 570-591 0.0093 0.0083 0.0115 0.0076 0.00 0.0%
Orange 591-610 0.0100 0.0107 0.0092 0.0114 0.00 0.0%
Red 610-760 0.0051 0.0096 0.0031 0.0110 0.00 0.0%
total (400-700) 43.50 43.51 43.64 43.73 13.09 100.0%
TABLE 4
Fiber 3 - with Sodium Bicarbonate in Lurol Oil
Fiber 3- with Sodium mW/cm2 at 5 cm
Bicarbonate in Lurol Oil 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 45.77 45.38 45.39 45.41 45.38 45.46 45.53
Fluoresc. 519-760 0.03 0.03 0.03 0.02 0.03 0.03 0.02
total 400-760 45.79708 45.4078 45.42176 45.43369 45.40676 45.48801 45.55223
% fluorescence 0.1% 0.1% 0.1% 0.0% 0.1% 0.1% 0.0%
purple (400)-450  30.4595 29.6024 29.2516 28.8436 28.6273 28.4034 28.2416
Blue 450-500 15.2759 15.7454 16.1074 16.5308 16.7115 17.0158 17.2490
Green 500-570 0.0356 0.0341 0.0350 0.0419 0.0480 0.0437 0.0514
Yellow 570-591 0.0075 0.0081 0.0062 0.0067 0.0080 0.0068 0.0031
Orange 591-610 0.0107 0.0106 0.0104 0.0063 0.0071 0.0089 0.0040
Red 610-760 0.0082 0.0076 0.0117 0.0046 0.0051 0.0098 0.0035
total (400-700) 45.80 45.41 45.42 45.43 45.41 45.49 45.55
Fiber 3- with Sodium mW/cm2 at 5 cm
Bicarbonate in Lurol Oil 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 45.55 45.53 45.53 45.64 13.65 99.9%
Fluoresc. 519-760 0.03 0.04 0.02 0.03 0.01 0.1%
total 400-760 45.58 45.56858 45.554 45.66506 13.66 100.0%
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.00 0.1%
purple (400)-450  28.0332 27.8598 27.6870 27.6032 8.61 63.0%
Blue 450-500 17.4738 17.6294 17.7953 17.9823 5.03 36.8%
Green 500-570 0.0500 0.0491 0.0580 0.0645 0.01 0.1%
Yellow 570-591 0.0094 0.0100 0.0052 0.0053 0.00 0.0%
Orange 591-610 0.0090 0.0116 0.0060 0.0060 0.00 0.0%
Red 610-760 0.0049 0.0091 0.0026 0.0041 0.00 0.0%
total (400-700) 45.58 45.57 45.55 45.67 13.66 100.0%
TABLE 5
Photoactivatable fibers comprising
polylactic acid (PLA) compounded with Eosin
Fluorescence
Fiber Composition Emission
5 PLA with 0.5% Eosin + Lurol Oil Coating Table 6
6 PLA with 0.5% Eosin + 1% Urea Peroxide Table 7
Coating + Lurol Oil Coating
7 PLA with 0.5% Eosin + Sodium Bicarbonate Table 8
Coating + Lurol Oil Coating
TABLE 6
Fiber 5 - Polylactic Acid + Eosin Inside, Lurol Oil Outside
Fiber 5 - Polylactic
Acid + Eosin Inside, mW/cm2 at 5 cm
Lurol Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 14.94 14.93 14.85 14.75 14.71 14.67 14.65
Fluoresc. 519-760 1.12 1.02 0.98 0.95 0.94 0.92 0.91
total 400-760 16.05383 15.94828 15.82929 15.69884 15.6478 15.58449 15.56786
% fluorescence 6.9% 6.4% 6.2% 6.1% 6.0% 5.9% 5.9%
purple (400)-450  10.4182 10.2214 10.0756 9.9133 9.8031 9.7045 9.6358
Blue 450-500 4.5199 4.7079 4.7777 4.8335 4.9048 4.9608 5.0190
Green 500-570 0.1184 0.1103 0.1017 0.0982 0.0979 0.0945 0.0947
Yellow 570-591 0.2998 0.2848 0.2731 0.2668 0.2631 0.2578 0.2561
Orange 591-610 0.3337 0.3119 0.3002 0.2939 0.2891 0.2839 0.2806
Red 610-760 0.3793 0.3265 0.3152 0.3070 0.3035 0.2965 0.2949
total (400-700) 16.07 15.96 15.84 15.71 15.66 15.60 15.58
Fiber 5 - Polylactic
Acid + Eosin Inside, mW/cm2 at 5 cm
Lurol Oil Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 14.66 14.62 14.61 14.61 4.42 93.9%
Fluoresc. 519-760 0.90 0.87 0.87 0.85 0.28 6.0%
total 400-760 15.55919 15.48759 15.48833 15.46502 4.71 99.9%
% fluorescence 5.8% 5.6% 5.6% 5.5% 0.06 6.0%
purple (400)-450  9.5792 9.5010 9.4528 9.4132 2.95 62.6%
Blue 450-500 5.0769 5.1140 5.1618 5.1980 1.47 31.3%
Green 500-570 0.0931 0.0908 0.0913 0.0890 0.03 0.6%
Yellow 570-591 0.2523 0.2461 0.2436 0.2386 0.08 1.7%
Orange 591-610 0.2780 0.2700 0.2688 0.2626 0.09 1.9%
Red 610-760 0.2929 0.2784 0.2828 0.2761 0.09 2.0%
total (400-700) 15.57 15.50 15.50 15.48 4.71 100.0%
TABLE 7
Fiber 6 - Polylactic Acid + Eosin Inside, UP + Lurol Oil Outside
Fiber 6 - Polylactic
Acid + Eosin Inside,
UP + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 15.27 15.32 15.33 15.31 15.29 15.28 15.26
Fluoresc. 519-760 1.05 0.94 0.91 0.90 0.89 0.86 0.85
total 400-760 16.32258 16.26344 16.24112 16.20668 16.17224 16.14035 16.10769
% fluorescence 6.4% 5.8% 5.6% 5.6% 5.5% 5.3% 5.3%
purple (400)-450  10.6935 10.4773 10.3672 10.2573 10.1656 10.0862 10.0081
Blue 450-500 4.5788 4.8458 4.9628 5.0482 5.1215 5.1921 5.2499
Green 500-570 0.0972 0.0853 0.0822 0.0826 0.0797 0.0787 0.0778
Yellow 570-591 0.2906 0.2567 0.2470 0.2436 0.2380 0.2330 0.2287
Orange 591-610 0.3265 0.2930 0.2836 0.2786 0.2726 0.2664 0.2618
Red 610-760 0.3516 0.3193 0.3121 0.3097 0.3079 0.2968 0.2942
total (400-700) 16.34 16.28 16.25 16.22 16.19 16.15 16.12
Fiber 6 - Polylactic
Acid + Eosin Inside,
UP + Lurol Oil mW/cm2 at 5 cm
Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 15.22 15.18 15.14 15.11 4.58 94.4%
Fluoresc. 519-760 0.83 0.83 0.80 0.79 0.27 5.5%
total 400-760 16.05246 16.00419 15.94197 15.8982 4.84 99.9%
% fluorescence 5.2% 5.2% 5.0% 5.0% 0.05 5.5%
purple (400)-450  9.9236 9.8464 9.7768 9.7092 3.05 62.9%
Blue 450-500 5.2948 5.3311 5.3629 5.3990 1.53 31.6%
Green 500-570 0.0752 0.0752 0.0741 0.0737 0.02 0.5%
Yellow 570-591 0.2254 0.2223 0.2162 0.2132 0.07 1.5%
Orange 591-610 0.2578 0.2549 0.2474 0.2433 0.08 1.7%
Red 610-760 0.2880 0.2866 0.2764 0.2715 0.09 1.9%
total (400-700) 16.06 16.02 15.95 15.91 4.85 100.0%
TABLE 8
Fiber 7 - Polylactic Acid + Eosin Inside, Bicarb + Lurol Oil Outside
Fiber 7 - Polylactic
Acid + Eosin Inside,
Bicarb + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 16.07 16.04 16.01 15.90 15.79 15.77 15.72
Fluoresc. 519-760 1.12 0.99 0.96 0.93 0.92 0.92 0.91
total 400-760 17.18991 17.03564 16.96755 16.83133 16.71217 16.69256 16.62935
% fluorescence 6.5% 5.8% 5.7% 5.5% 5.5% 5.5% 5.4%
purple (400)-450  11.1705 10.9276 10.8025 10.6200 10.4800 10.3930 10.2891
Blue 450-500 4.9016 5.1169 5.2034 5.2792 5.3112 5.3811 5.4351
Green 500-570 0.1197 0.1019 0.0951 0.0932 0.0913 0.0929 0.0918
Yellow 570-591 0.3141 0.2730 0.2662 0.2585 0.2557 0.2532 0.2495
Orange 591-610 0.3475 0.3054 0.2967 0.2881 0.2847 0.2817 0.2778
Red 610-760 0.3529 0.3253 0.3178 0.3062 0.3028 0.3042 0.2994
total (400-700) 17.21 17.05 16.98 16.85 16.73 16.71 16.64
Fiber 7 - Polylactic
Acid + Eosin Inside,
Bicarb + Lurol Oil mW/cm2 at 5 cm
Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 15.6 15.6 15.70 15.75 4.75 94.3%
Fluoresc. 519-760 0.89 0.87 0.87 0.84 0.28 5.6%
total 400-760 16.55821 16.5202 16.56995 16.59658 5.03 99.9%
% fluorescence 5.4% 5.2% 5.2% 5.1% 0.06 5.6%
purple (400)-450  10.1908 10.1298 10.1080 10.0959 3.15 62.6%
Blue 450-500 5.4730 5.5252 5.5922 5.6575 1.60 31.7%
Green 500-570 0.0894 0.0859 0.0890 0.0858 0.03 0.6%
Yellow 570-591 0.2454 0.2382 0.2381 0.2313 0.08 1.5%
Orange 591-610 0.2740 0.2670 0.2655 0.2586 0.09 1.7%
Red 610-760 0.2988 0.2868 0.2898 0.2799 0.09 1.8%
total (400-700) 16.57 16.53 16.58 16.61 5.04 100.0%
TABLE 9
Photoactivatable fibers comprising
polypropylene compounded with Eosin
Fluorescence
Fiber Composition Emission
8 Polypropylene with 0.5% Eosin + Lurol Oil Coating Table 10
9 Polypropylene with 0.5% Eosin + 1% Urea Peroxide Table 11
Coating + Lurol Oil Coating
10 Polypropylene with 0.5% Eosin + Sodium Table 12
Bicarbonate Coating + Lurol Oil Coating
11 Polypropylene with 0.5% Eosin + 10 g/L Eosin Y Table 13
Coating + Lurol Oil Coating
TABLE 10
Fiber 8 - Polypropylene + Eosin Inside, Lurol Oil Outside
Fiber 8 - Polypropylene + mW/cm2 at 5 cm
Eosin Inside, Lurol Oil 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 38.79 38.50 38.31 38.11 37.91 37.60 37.37
Fluoresc. 519-760 0.10 0.01 0.01 0.01 0.01 0.01 0.01
total 400-760 38.887 38.51682 38.31451 38.11967 37.91618 37.60603 37.37597
% fluorescence 0.2% 0.0% 0.0% 0.0% 0.0% 0.0% 0.0%
purple (400)-450  26.213 25.6104 25.2140 24.8144 24.4722 24.0801 23.7486
Blue 450-500 12.5660 12.8714 13.0711 13.2695 13.4083 13.4929 13.5901
Green 500-570 0.01 0.0223 0.0221 0.0249 0.0289 0.0253 0.0293
Yellow 570-591 0.0002 0.0003 0.0006 0.0053 0.0014 0.0036 0.0021
Orange 591-610 0.00 0.0029 0.0044 0.0049 0.0026 0.0031 0.0030
Red 610-760 0.09 0.0096 0.0026 0.0008 0.0029 0.0012 0.0029
total (400-700) 38.89 38.52 38.31 38.12 37.92 37.61 37.38
Fiber 8 - Polypropylene + mW/cm2 at 5 cm
Eosin Inside, Lurol Oil 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 37.23 36.98 36.89 36.70 11.33 99.9%
Fluoresc. 519-760 0.01 0.01 0.02 0.02 0.01 0.1%
total 400-760 37.24258 36.99724 36.90971 36.7173 11.34 100.0
% fluorescence 0.0% 0.0% 0.1% 0.1% 0.00 0.1%
purple (400)-450  23.5275 23.2268 23.0455 22.8148 7.32 64.6%
Blue 450-500 13.6822 13.7305 13.8151 13.8517 4.00 35.3%
Green 500-570 0.0257 0.0272 0.0345 0.0339 0.01 0.1
Yellow 570-591 0.0010 0.0023 0.0053 0.0030 0.00 0.0%
Orange 591-610 0.0033 0.0045 0.0032 0.0054 0.00 0.0
Red 610-760 0.0029 0.0061 0.0060 0.0087 0.00 0.0
total (400-700) 37.24 37.00 36.91 36.72 11.34 100.0%
TABLE 11
Fiber 9 - Polypropylene + Eosin Inside, UP + Lurol Oil Outside
Fiber 9 - Polypropylene +
Eosin Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 mi 1 min 1.5 min 2 mi 2.5 min 3 min
Lamp 400-518 38.22 37.85 37.66 37.36 37.11 36.88 36.72
Fluoresc. 519-760 0.12 0.00 0.02 0.00 0.01 0.01 0.02
total 400-760 38.33982 37.8572 37.67632 37.36189 37.1219 36.89308 36.73885
% fluorescence 0.3% 0.0% 0.0% 0.0% 0.0% 0.0% 0.0%
purple (400)-450  25.9945 25.2982 24.9107 24.4318 24.0608 23.7143 23.4416
Blue 450-500 12.2258 12.535 12.7280 12.9008 13.030 13.1446 13.2552
Green 500-570 0.0032 0.0220 0.0210 0.0265 0.0273 0.0230 0.0278
Yellow 570-591 0.0007 0.0001 0.0038 0.0005 0.0004 0.0048 0.0034
Orange 591-610 0.0005 0.0003 0.0053 0.0021 0.0014 0.0052 0.0048
Red 610-760 0.1152 0.0014 0.0078 0.0002 0.0014 0.0014 0.0062
total (400-700) 38.34 37.86 37.68 37.36 37.12 36.89 36.74
Fiber 9 - Polypropylene +
Eosin Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 3.5 min 4 min 4.5 min 5 min J/cm
Lamp 400-518 36.64 36.51 36.43 36.37 11.14 99.9%
Fluoresc. 519-760 0.01 0.01 0.01 0.01 0.01 0.1%
total 400-760 36.64907 36.52148 36.44165 36.37409 11.15 100.0%
% fluorescence 0.0% 0.0% 0.0% 0.0% 0.00 0.1%
purple (400)-450  23.2361 23.0084 22.8281 22.6777 7.23 64.8%
Blue 450-500 13.3760 13.4809 13.5761 13.6610 3.91 35.1%
Green 500-570 0.0285 0.0241 0.0321 0.0306 0.01 0.1%
Yellow 570-591 0.0005 0.0029 0.0011 0.0009 0.00 0.0%
Orange 591-610 0.0033 0.0033 0.0025 0.0023 0.00 0.0%
Red 610-760 0.0048 0.0020 0.0019 0.0017 0.00 0.0%
total (400-700) 36.65 36.52 36.44 36.37 11.15 100.0%
TABLE 12
Fiber 10 - Polypropylene + Eosin Inside, Bicarb + Lurol Oil Outside
Fiber 10 -
Polypropylene + Eosin mW/cm2 at 5 cm
Inside, Bicarb + Lurol Oil 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 36.92 36.59 36.47 36.29 36.17 36.04 35.91
Fluoresc. 519-760 0.00 0.01 0.01 0.01 0.01 0.01 0.01
total 400-760 36.92294 36.59499 36.47866 36.30052 36.18347 36.04749 35.91653
% fluorescence 0.0% 0.0% 0.0% 0.0% 0.0% 0.0% 0.0%
purple (400)-450  24.9566 24.3430 24.0409 23.6970 23.4067 23.1523 22.8998
Blue 450-500 11.9414 12.2264 12.4073 12.5720 12.7439 12.8609 12.9852
Green 500-570 0.0226 0.0177 0.0253 0.0257 0.0262 0.0254 0.0258
Yellow 570-591 0.0012 0.0030 0.0017 0.0041 0.0026 0.0015 0.0031
Orange 591-610 0.0010 0.0035 0.0012 0.0015 0.0027 0.0031 0.0023
Red 610-760 0.0001 0.0015 0.0022 0.0002 0.0014 0.0043 0.0004
total (400-700) 36.92 36.60 36.48 36.30 36.18 36.05 35.92
Fiber 10 -
Polypropylene + Eosin mW/cm2 at 5 cm
Inside, Bicarb + Lurol Oil 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 35.83 35.76 35.70 35.67 10.85 100.0%
Fluoresc. 519-760 0.01 0.01 0.01 0.01 0.00 0.0%
total 400-760 35.84232 35.77078 35.70893 35.67485 10.85 100.0%
% fluorescence 0.0% 0.0% 0.0% 0.0% 0.00 0.0%
purple (400)-450  22.7089 22.5307 22.3735 22.2601 7.02 64.7%
Blue 450-500 13.1015 13.2040 13.3008 13.3833 3.82 35.2%
Green 500-570 0.0244 0.0253 0.0297 0.0281 0.01 0.1%
Yellow 570-591 0.0012 0.0039 0.0036 0.0006 0.00 0.0%
Orange 591-610 0.0031 0.0046 0.0013 0.0012 0.00 0.0%
Red 610-760 0.0033 0.0024 0.0000 0.0015 0.00 0.0%
total (400-700) 35.84 35.77 35.71 35.67 10.85 100.0%
TABLE 13
Fiber 11 - Polypropylene + Eosin Inside, Eosin + Lurol Oil Outside
Fiber 11 - Polypropylene +
Eosin Inside, Eosin + Lurol mW/cm2 at 5 cm
Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 34.92 34.27 34.10 33.96 33.80 33.65 33.52
Fluoresc. 519-760 0.04 0.02 0.03 0.03 0.03 0.03 0.03
total 400-760 34.96027 34.29043 34.12328 33.98972 33.83178 33.67762 33.55483
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.1% 0.1% 0.1%
purple (400)-450  24.0092 23.0633 22.6970 22.3805 22.0694 21.8103 21.5672
Blue 450-500 10.9008 11.1891 11.3868 11.5594 11.7112 11.8201 11.9385
Green 500-570 0.0173 0.0173 0.0143 0.0207 0.0223 0.0225 0.0194
Yellow 570-591 0.0118 0.0090 0.0071 0.0088 0.0095 0.0102 0.0076
Orange 591-610 0.0114 0.0076 0.0097 0.0112 0.0104 0.0078 0.0109
Red 610-760 0.0102 0.0044 0.0088 0.0097 0.0095 0.0069 0.0117
total (400-700) 34.96 34.29 34.12 33.99 33.83 33.68 33.56
Fiber 11 - Polypropylene +
Eosin Inside, Eosin + Lurol mW/cm2 at 5 cm
Oil Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 33.43 33.36 33.23 33.16 10.15 99.9%
Fluoresc. 519-760 0.03 0.03 0.03 0.03 0.01 0.1%
total 400-760 33.45521 33.38872 33.26012 33.18787 10.16 100.0%
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.00 0.1%
purple (400)-450  21.3650 21.1855 20.9851 20.8562 6.63 65.3%
Blue 450-500 12.0429 12.1567 12.2284 12.2886 3.51 34.5%
Green 500-570 0.0232 0.0196 0.0235 0.0199 0.01 0.1%
Yellow 570-591 0.0079 0.0079 0.0075 0.0085 0.00 0.0%
Orange 591-610 0.0081 0.0096 0.0079 0.0085 0.00 0.0%
Red 610-760 0.0082 0.0098 0.0081 0.0065 0.00 0.0%
total (400-700) 33.46 33.39 33.26 33.19 10.16 100.0%
TABLE 14
Photoactivatable fibers comprising nylon compounded with Eosin
Fluorescence
Fiber Composition Emission
12 Nylon with 0.5% Eosin + Lurol Oil Coating Table 15
13 Nylon with 0.5% Eosin + 1% Urea Peroxide Table 16
Coating + Lurol Oil Coating
14 Nylon with 0.5% Eosin + Sodium Bicarbonate Table 17
Coating + Lurol Oil Coating
15 Nylon with 0.5% Eosin + 10 g/L Eosin Y Table 18
Coating + Lurol Oil Coating
TABLE 15
Fiber 12 - Nylon + Eosin Inside, Lurol Oil Outside
Fiber 12 - Nylon + Eosin mW/cm2 at 5 cm
Inside, Lurol Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 8.45 9.13 10.34 11.38 12.24 13.06 13.83
Fluoresc. 519-760 7.55 6.46 5.97 5.54 5.23 4.91 4.64
total 400-760 15.99847 15.59112 16.31268 16.92697 17.46969 17.96796 18.46997
% fluorescence 47.2% 41.4% 36.6% 32.7% 29.9% 27.3% 25.1%
purple (400)-450  6.8019 6.9690 7.5393 7.9927 8.3430 8.6685 8.9554
Blue 450-500 1.6408 2.1589 2.7965 3.3803 3.8857 4.3748 4.8527
Green 500-570 2.0031 1.7498 1.6586 1.5746 1.5063 1.4374 1.3732
Yellow 570-591 2.2768 1.9007 1.7088 1.5559 1.4441 1.3456 1.2576
Orange 591-610 1.4927 1.2519 1.1345 1.0406 0.9709 0.9120 0.8536
Red 610-760 1.8387 1.6080 1.5182 1.4229 1.3568 1.2651 1.2106
total (400-700) 16.05 15.64 16.36 16.97 17.51 18.00 18.50
Fiber 12 - Nylon + Eosin mW/cm2 at 5 cm
Inside, Lurol Oil Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 14.52 15.24 15.82 16.38 3.72 69.9%
Fluoresc. 519-760 4.40 4.25 4.03 3.90 1.59 29.9%
total 400-760 18.92674 19.48819 19.84828 20.28261 5.31 99.8%
% fluorescence 23.3% 21.8% 20.3% 19.2% 0.30 29.9%
purple (400)-450  9.2182 9.4951 9.6972 9.8883 2.51 47.2%
Blue 450-500 5.2897 5.7259 6.0989 6.4642 1.21 22.7%
Green 500-570 1.3144 1.2775 1.2280 1.2009 0.45 8.5%
Yellow 570-591 1.1845 1.1207 1.0606 1.0133 0.45 8.4%
Orange 591-610 0.8080 0.7702 0.7336 0.7040 0.30 5.6%
Red 610-760 1.1433 1.1291 1.0584 1.0397 0.41 7.6%
total (400-700) 18.96 19.52 19.88 20.31 5.32 100.0%
TABLE 16
Fiber 13 - Nylon + Eosin Inside, UP + Lurol Oil Outside (25-30 minutes)
Fiber 13 - Nylon +
Eosin Inside, UP +
Lurol Oil Outside (25-30 mW/cm2 at 5 cm
minutes) 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 24.96 25.05 25.19 25.29 25.42 25.49 25.61
Fluoresc. 519-760 1.98 1.93 1.93 1.95 1.91 1.90 1.89
total 400-760 26.93968 26.98401 27.11688 27.24167 27.32461 27.38227 27.49843
% fluorescence 7.4% 7.2% 7.1% 7.2% 7.0% 6.9% 6.9%
purple (400)-450  13.4292 13.4647 13.5354 13.5872 13.6501 13.6725 13.7437
Blue 450-500 11.4229 11.4809 11.5418 11.5944 11.6551 11.7014 11.7509
Green 500-570 0.7422 0.7341 0.7330 0.7372 0.7289 0.7264 0.7299
Yellow 570-591 0.4073 0.3998 0.3982 0.3978 0.3923 0.3909 0.3853
Orange 591-610 0.3298 0.3235 0.3230 0.3212 0.3183 0.3170 0.3128
Red 610-760 0.6231 0.5954 0.5999 0.6183 0.5943 0.5883 0.5899
total (400-700) 26.95 27.00 27.13 27.26 27.34 27.40 27.51
Fiber 13 - Nylon +
Eosin Inside, UP +
Lurol Oil Outside (25-30 mW/cm2 at 5 cm
minutes) 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 25.68 25.78 25.90 25.99 7.63 93.0%
Fluoresc. 519-760 1.84 1.88 1.86 1.84 0.57 7.0%
total 400-760 27.52573 27.66029 27.7626 27.83434 8.20 99.9%
% fluorescence 6.7% 6.8% 6.7% 6.6% 0.07 7.0%
purple (400)-450  13.7672 13.8125 13.8662 13.9151 4.10 49.9%
Blue 450-500 11.8032 11.8555 11.9193 11.9667 3.50 42.7%
Green 500-570 0.7229 0.7323 0.7294 0.7230 0.22 2.7%
Yellow 570-591 0.3833 0.3793 0.3786 0.3737 0.12 1.4%
Orange 591-610 0.3103 0.3079 0.3066 0.3036 0.10 1.2%
Red 610-760 0.5528 0.5867 0.5762 0.5659 0.18 2.2%
total (400-700) 27.54 27.67 27.78 27.85 8.21 100.0%
TABLE 17
Fiber 14 - Nylon + Eosin Inside, Bicarbonate + Lurol Oil Outside (25-30 minutes)
Fiber 14 - Nylon +
Eosin Inside,
Bicarbonate + Lurol Oil
Outside (25-30 mW/cm2 at 5 cm
minutes) 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 27.04 27.10 27.20 27.13 27.12 27.21 27.30
Fluoresc. 519-760 1.72 1.70 1.69 1.65 1.61 1.59 1.59
total 400-760 28.7625 28.80483 28.88949 28.77401 28.72682 28.79745 28.89051
% fluorescence 6.0% 5.9% 5.8% 5.7% 5.6% 5.5% 5.5%
purple (400)-450  14.7774 14.7599 14.7845 14.7271 14.6997 14.7221 14.7524
Blue 450-500 12.1575 12.2336 12.3042 12.2857 12.3044 12.3716 12.4369
Green 500-570 0.7817 0.7752 0.7711 0.7525 0.7403 0.7425 0.7407
Yellow 570-591 0.3552 0.3522 0.3484 0.3332 0.3294 0.3225 0.3216
Orange 591-610 0.2653 0.2623 0.2593 0.2496 0.2476 0.2397 0.2398
Red 610-760 0.4370 0.4330 0.4333 0.4369 0.4162 0.4097 0.4097
total (400-700) 28.77 28.82 28.90 28.78 28.74 28.81 28.90
Fiber 14 - Nylon +
Eosin Inside,
Bicarbonate + Lurol Oil
Outside (25-30 mW/cm2 at 5 cm
minutes) 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 27.37 27.49 27.58 27.53 8.18 94.4%
Fluoresc. 519-760 1.57 1.54 1.56 1.49 0.49 5.6%
total 400-760 28.94176 29.02669 29.14196 29.0172 8.66 100.0%
% fluorescence 5.4% 5.3% 5.3% 5.1% 0.06 5.6%
purple (400)-450  14.7707 14.8138 14.8509 14.7998 4.43 51.1%
Blue 450-500 12.4876 12.5577 12.6191 12.6099 3.71 42.8%
Green 500-570 0.7376 0.7291 0.7282 0.7190 0.22 2.6%
Yellow 570-591 0.3195 0.3133 0.3150 0.3054 0.10 1.1%
Orange 591-610 0.2385 0.2326 0.2365 0.2263 0.07 0.9%
Red 610-760 0.3982 0.3904 0.4027 0.3666 0.13 1.4%
total (400-700) 28.95 29.04 29.15 29.03 8.67 100.0%
TABLE 18
Fiber 15 - Nylon + Eosin Inside, Eosin + Lurol Oil Outside - Trial 2 (25-30 minutes)
Fiber 15 - Nylon + Eosin
Inside, Eosin + Lurol Oil
Outside - Trial 2 (25-30 mW/cm2 at 5 cm
minutes) 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 18.95 19.06 19.19 19.29 19.41 19.49 19.61
Fluoresc. 519-760 2.25 2.23 2.24 2.19 2.20 2.17 2.18
total 400-760 21.20136 21.28697 21.42811 21.48191 21.60579 21.66376 21.78431
% fluorescence 10.6% 10.5% 10.4% 10.2% 10.2% 10.0% 10.0%
purple (400)-450  10.4090 10.4463 10.5206 10.5657 10.6302 10.6576 10.7182
Blue 450-500 8.4999 8.5673 8.6248 8.6759 8.7348 8.7871 8.8430
Green 500-570 0.5179 0.5198 0.5227 0.5133 0.5139 0.5128 0.5124
Yellow 570-591 0.5174 0.5138 0.5096 0.5043 0.5029 0.4997 0.4990
Orange 591-610 0.4525 0.4474 0.4439 0.4396 0.4384 0.4349 0.4342
Red 610-760 0.8250 0.8123 0.8263 0.8028 0.8053 0.7911 0.7970
total (400-700) 21.22 21.31 21.45 21.50 21.63 21.68 21.80
Fiber 15 - Nylon + Eosin
Inside, Eosin + Lurol Oil
Outside - Trial 2 (25-30 mW/cm2 at 5 cm
minutes) 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 19.74 19.83 19.94 20.05 5.84 89.8%
Fluoresc. 519-760 2.19 2.15 2.15 2.13 0.66 10.1%
total 400-760 21.92765 21.98483 22.08331 22.17704 6.49 99.9%
% fluorescence 10.0% 9.8% 9.7% 9.6% 0.10 10.1%
purple (400)-450  10.7853 10.8302 10.8776 10.9295 3.19 49.1%
Blue 450-500 8.9077 8.9536 9.0093 9.0661 2.63 40.4%
Green 500-570 0.5241 0.5177 0.5155 0.5159 0.16 2.4%
Yellow 570-591 0.4989 0.4941 0.4892 0.4894 0.15 2.3%
Orange 591-610 0.4322 0.4282 0.4264 0.4245 0.13 2.0%
Red 610-760 0.7988 0.7803 0.7846 0.7707 0.24 3.7%
total (400-700) 21.95 22.00 22.10 22.20 6.50 100.0%
TABLE 19
Photoactivatable fibers comprising polybutylene
terephthalate (PBT) compounded with Eosin
Fluorescence
Fiber Composition Emission
16 Virgin PBT + Lurol Oil Coating Table 20
17 PBT with 1% Eosin + Lurol Oil Coating Table 21
18 PBT with 1% Eosin + 1% Urea Peroxide Table 22
Coating + Lurol Oil Coating
19 PBT with 1% Eosin + Sodium Bicarbonate Table 23
Coating + Lurol Oil Coating
20 PBT with 1% Eosin + 10 g/L Eosin Y Coating + Table 24
Lurol Oil Coating
TABLE 20
Fiber 16 - PBT Blank
Fiber 16 - PBT mW/cm2 at 5 cm
Blank 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 69.78 69.35 69.24 68.90 68.53 68.16 68.04
Fluoresc. 519-760 0.05 0.07 0.06 0.05 0.05 0.06 0.05
total 400-760 69.82895 69.4195 69.30044 68.95217 68.5783 68.21259 68.09006
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.1% 0.1% 0.1%
purple (400)-450  42.9096 42.0190 41.5394 40.9650 40.4537 39.9428 39.6390
Blue 450-500 26.7852 27.2232 27.5890 27.8149 27.9591 28.0905 28.2822
Green 500-570 0.1043 0.1571 0.1564 0.1587 0.1566 0.1574 0.1648
Yellow 570-591 0.0000 0.0052 0.0084 0.0098 0.0050 0.0067 0.0040
Orange 591-610 0.0000 0.0088 0.0059 0.0033 0.0035 0.0087 0.0001
Red 610-760 0.0299 0.0066 0.0016 0.0006 0.0006 0.0071 0.0000
total (400-700) 69.83 69.42 69.30 68.95 68.58 68.21 68.09
Fiber 16 - PBT mW/cm2 at 5 cm
Blank 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 67.72 67.51 67.29 67.15 20.54 99.9%
Fluoresc. 519-760 0.07 0.06 0.05 0.04 0.02 0.1%
total 400-760 67.79068 67.56456 67.3467 67.19618 20.55 100.0%
% fluorescence 0.1% 0.1% 0.1% 0.1% 0.00 0.1%
purple (400)-450  39.2507 38.9616 38.6804 38.4675 12.13 59.0%
Blue 450-500 28.3575 28.4216 28.4878 28.5608 8.37 40.7%
Green 500-570 0.1639 0.1680 0.1621 0.1529 0.05 0.2%
Yellow 570-591 0.0110 0.0079 0.0106 0.0061 0.00 0.0%
Orange 591-610 0.0069 0.0049 0.0058 0.0060 0.00 0.0%
Red 610-760 0.0010 0.0006 0.0001 0.0032 0.00 0.0%
total (400-700) 67.79 67.56 67.35 67.20 20.55 100.0%
TABLE 21
Fiber 17 - PBT + Eosin Inside, Lurol Oil Outside
Fiber 17 - PBT + Eosin UZ,13/49 mW/cm2 at 5 cm
Inside, Lurol Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 2.63 2.57 2.41 2.18 2.06 1.99 2.26
Fluoresc. 519-760 2.83 2.73 2.71 2.64 2.58 2.51 2.45
total 400-760 5.463108 5.298557 5.120492 4.828287 4.644863 4.504063 4.707606
% fluorescence 51.8% 51.5% 53.0% 54.8% 55.6% 55.8% 52.1%
purple (400)-450  1.8166 1.7553 1.6450 1.5014 1.4223 1.3755 1.5282
Blue 450-500 0.8139 0.8126 0.7602 0.6817 0.6405 0.6139 0.7270
Green 500-570 0.0536 0.0543 0.0575 0.0548 0.0545 0.0552 0.0543
Yellow 570-591 0.5284 0.4851 0.4763 0.4619 0.4510 0.4395 0.4304
Orange 591-610 0.7208 0.6774 0.6674 0.6502 0.6344 0.6149 0.5997
Red 610-760 1.5646 1.5467 1.5464 1.5100 1.4731 1.4350 1.3972
total (400-700) 5.50 5.33 5.15 4.86 4.68 4.53 4.74
Fiber 17 - PBT + Eosin mW/cm2 at 5 cm
Inside, Lurol Oil Outside 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 2.34 2.30 2.28 2.24 0.69 47.1%
Fluoresc. 519-760 2.40 2.36 2.34 2.33 0.77 52.3%
total 400-760 4.736382 4.659129 4.616988 4.571799 1.46 99.4%
% fluorescence 50.6% 50.7% 50.7% 50.9% 0.53 52.6%
purple (400)-450  1.5655 1.5335 1.5147 1.4931 0.47 32.0%
Blue 450-500 0.7718 0.7606 0.7591 0.7499 0.22 15.0%
Green 500-570 0.0554 0.0537 0.0556 0.0561 0.02 1.1%
Yellow 570-591 0.4193 0.4146 0.4093 0.4090 0.14 9.2%
Orange 591-610 0.5842 0.5764 0.5684 0.5648 0.19 12.9%
Red 610-760 1.3685 1.3481 1.3375 1.3262 0.44 29.7%
total (400-700) 4.76 4.69 4.64 4.60 1.47 100.0%
TABLE 22
Fiber 18 - PBT + Eosin Inside, UP + Lurol Oil Outside
Fiber 18 - PBT + Eosin
Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 0.42 0.46 1.12 0.91 0.91 0.96
Fluoresc. 519-760 2.32 2.04 1.90 1.84 1.81 1.78
total 400-760 2.740057 2.495696 3.021197 2.744473 2.727173 2.740978
% fluorescence 84.6% 81.8% 63.0% 66.9% 66.5% 65.1%
purple (400)-450  0.3091 0.3171 0.7094 0.5882 0.5908 0.6157
Blue 450-500 0.1126 0.1379 0.4059 0.3184 0.3210 0.3396
Green 500-570 0.0497 0.0412 0.0447 0.0430 0.0441 0.0444
Yellow 570-591 0.4315 0.3609 0.3414 0.3298 0.3247 0.3202
Orange 591-610 0.5479 0.4794 0.4456 0.4291 0.4212 0.4130
Red 610-760 1.3154 1.1822 1.0955 1.0564 1.0456 1.0277
total (400-700) 2.77 2.52 3.04 2.76 2.75 2.76
Fiber 18 - PBT + Eosin
Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 0.99 0.99 0.99 1.08 1.07 0.26 32.0%
Fluoresc. 519-760 1.76 1.72 1.69 1.66 1.63 0.56 67.2%
total 400-760 2.744468 2.71341 2.678671 2.743669 2.696495 0.82 99.3%
% fluorescence 64.0% 63.4% 63.1% 60.6% 60.3% 0.68 67.7%
purple (400)-450  0.6325 0.6333 0.6306 0.6807 0.6734 0.17 20.7%
Blue 450-500 0.3549 0.3580 0.3572 0.3990 0.3955 0.09 11.3%
Green 500-570 0.0452 0.0456 0.0463 0.0471 0.0470 0.01 1.6%
Yellow 570-591 0.3163 0.3103 0.3053 0.3009 0.2959 0.10 12.1%
Orange 591-610 0.4054 0.3958 0.3873 0.3800 0.3715 0.13 15.6%
Red 610-760 1.0096 0.9893 0.9704 0.9539 0.9309 0.32 38.6%
total (400-700) 2.76 2.73 2.70 2.76 2.71 0.83 100.0%
TABLE 23
Fiber 19 - PBT + Eosin Inside, Bicarb + Lurol Oil Outside
Fiber 19 - PBT + Eosin
Inside, Bicarb + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 0.55 0.56 1.00 1.17 1.25 1.08
Fluoresc. 519-760 2.40 2.11 1.94 1.86 1.78 1.76
total 400-760 2.954142 2.667009 2.942724 3.028633 3.035268 2.841185
% fluorescence 81.4% 79.1% 65.9% 61.5% 58.7% 62.1%
purple (400)-450  0.3923 0.3886 0.6557 0.7512 0.7970 0.6904
Blue 450-500 0.1566 0.1676 0.3467 0.4136 0.4562 0.3852
Green 500-570 0.0504 0.0408 0.0409 0.0416 0.0404 0.0425
Yellow 570-591 0.4400 0.3607 0.3312 0.3199 0.3066 0.3023
Orange 591-610 0.5668 0.4937 0.4519 0.4318 0.4119 0.4049
Red 610-760 1.3750 1.2394 1.1382 1.0913 1.0431 1.0353
total (400-700) 2.98 2.69 2.96 3.05 3.06 2.86
Fiber 19 - PBT + Eosin
Inside, Bicarb + Lurol Oil mW/cm2 at 5 cm
Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 1.05 1.05 1.09 1.11 1.13 0.30 34.4%
Fluoresc. 519-760 1.74 1.71 1.69 1.66 1.64 0.56 64.9%
total 400-760 2.787107 2.766328 2.777914 2.770098 2.774827 0.86 99.3%
% fluorescence 62.4% 61.9% 60.9% 60.1% 59.2% 0.65 65.3%
purple (400)-450  0.6687 0.6707 0.6870 0.6962 0.7091 0.19 22.2%
Blue 450-500 0.3775 0.3828 0.3989 0.4086 0.4225 0.10 12.1%
Green 500-570 0.0432 0.0441 0.0449 0.0453 0.0460 0.01 1.5%
Yellow 570-591 0.2983 0.2935 0.2904 0.2869 0.2834 0.10 11.2%
Orange 591-610 0.3978 0.3895 0.3835 0.3768 0.3705 0.13 15.0%
Red 610-760 1.0207 1.0044 0.9917 0.9744 0.9612 0.33 37.9%
total (400-700) 2.81 2.79 2.80 2.79 2.79 0.86 100.0%
TABLE 24
Fiber 20 - PBT + Eosin Inside, Eosin + Lurol Oil Outside
Fiber 20 - PBT + Eosin
Inside, Eosin + Lurol mW/cm2 at 5 cm
Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 3.25 3.82 3.91 4.14 4.19 4.39
Fluoresc. 519-760 2.72 2.62 2.54 2.42 2.36 2.30
total 400-760 5.966188 6.441835 6.450766 6.557832 6.549098 6.694657
% fluorescence 45.6% 40.7% 39.4% 36.9% 36.0% 34.4%
purple (400)-450  2.1823 2.5014 2.5369 2.6563 2.6642 2.7716
Blue 450-500 1.0644 1.3131 1.3703 1.4781 1.5245 1.6190
Green 500-570 0.0508 0.0554 0.0585 0.0551 0.0556 0.0568
Yellow 570-591 0.4800 0.4340 0.4202 0.4071 0.3951 0.3860
Orange 591-610 0.6916 0.6422 0.6186 0.5936 0.5743 0.5586
Red 610-760 1.5314 1.5275 1.4769 1.3971 1.3637 1.3304
total (400-700) 6.00 6.47 6.48 6.59 6.58 6.72
Fiber 20 - PBT + Eosin
Inside, Eosin + Lurol mW/cm2 at 5 cm
Oil Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 4.35 4.30 4.27 4.27 4.24 1.23 62.9%
Fluoresc. 519-760 2.27 2.23 2.20 2.17 2.16 0.72 36.7%
total 400-760 6.622601 6.520864 6.46933 6.436219 6.394325 1.94 99.6%
% fluorescence 34.3% 34.1% 34.1% 33.7% 33.8% 0.37 36.8%
purple (400)-450  2.7308 2.6852 2.6568 2.6469 2.6211 0.78 40.1%
Blue 450-500 1.6181 1.6076 1.6056 1.6155 1.6114 0.44 22.8%
Green 500-570 0.0560 0.0546 0.0576 0.0569 0.0567 0.02 0.9%
Yellow 570-591 0.3797 0.3738 0.3682 0.3644 0.3631 0.12 6.2%
Orange 591-610 0.5488 0.5387 0.5300 0.5229 0.5176 0.17 9.0%
Red 610-760 1.3163 1.2875 1.2773 1.2554 1.2499 0.41 21.2%
total (400-700) 6.65 6.55 6.50 6.46 6.42 1.95 100.0%
TABLE 25
Photoactivatable fibers comprising poly(methyl
methacrylate) (PMMA) compounded with Eosin
Fluorescence
Fiber Composition Emission
21 PMMA with 1% Eosin + Lurol Oil Coating Table 26
22 PMMA with 1% Eosin + 1% Urea Peroxide Table 27
Coating + Lurol Oil Coating
23 PrMMA with 1% Eosin + Sodium Bicarbonate Table 28
Coating + Lurol Oil Coating
24 PMMA with 1% Eosin + 10 g/L Eosin Y Table 29
Coating + Lurol Oil Coating
TABLE 26
Fiber 21 - PMMA + Eosin Inside, Lurol Oil Outside
Fiber 21 - PMMA + Eosin mW/cm2 at 5 cm
Inside, Lurol Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 10.26 10.12 10.08 10.02 9.98 9.96
Fluoresc. 519-760 0.73 0.67 0.65 0.64 0.63 0.63
total 400-760 10.99377 10.79335 10.72893 10.65819 10.61231 10.58607
% fluorescence 6.7% 6.2% 6.0% 6.0% 5.9% 5.9%
purple (400)-450  7.8615 7.6370 7.5561 7.4510 7.3697 7.3017
Blue 450-500 2.3995 2.4856 2.5276 2.5694 2.6118 2.6571
Green 500-570 0.0096 0.0069 0.0050 0.0043 0.0038 0.0033
Yellow 570-591 0.1304 0.1195 0.1128 0.1092 0.1063 0.1037
Orange 591-610 0.2326 0.2175 0.2105 0.2074 0.2043 0.2022
Red 610-760 0.3732 0.3388 0.3284 0.3283 0.3277 0.3293
total (400-700) 11.01 10.81 10.74 10.67 10.62 10.60
Fiber 21 - PMMA + Eosin mW/cm2 at 5 cm
Inside, Lurol Oil Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 9.88 9.90 9.83 9.79 9.82 2.99 93.9%
Fluoresc. 519-760 0.61 0.60 0.60 0.60 0.59 0.19 6.0%
total 400-760 10.49542 10.50296 10.43348 10.39166 10.41602 3.19 99.9%
% fluorescence 5.9% 5.7% 5.8% 5.8% 5.7% 0.06 6.0%
purple (400)-450  7.2094 7.1832 7.1110 7.0489 7.0420 2.21 69.4%
Blue 450-500 2.6720 2.7161 2.7200 2.7422 2.7821 0.78 24.6%
Green 500-570 0.0028 0.0026 0.0025 0.0023 0.0020 0.00 0.0%
Yellow 570-591 0.1003 0.0978 0.0963 0.0953 0.0928 0.03 1.0%
Orange 591-610 0.1977 0.1949 0.1934 0.1922 0.1889 0.06 1.9%
Red 610-760 0.3241 0.3193 0.3211 0.3215 0.3190 0.10 3.1%
total (400-700) 10.51 10.51 10.44 10.40 10.43 3.19 100.0%
TABLE 27
Fiber 22 - PMMA + Eosin Inside, UP + Lurol Oil Outside
Fiber 22 - PMMA + Eosin
Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 15.69 14.95 14.74 14.59 14.47 14.42
Fluoresc. 519-760 0.75 0.67 0.66 0.64 0.64 0.63
total 400-760 16.4387 15.62283 15.39582 15.23084 15.11069 15.05078
% fluorescence 4.6% 4.3% 4.3% 4.2% 4.3% 4.2%
purple (400)-450  11.0082 10.3866 10.1416 9.9691 9.8076 9.7133
Blue 450-500 4.6795 4.5640 4.5964 4.6207 4.6597 4.7054
Green 500-570 0.0004 0.0004 0.0002 0.0000 0.0000 0.0000
Yellow 570-591 0.0950 0.0842 0.0818 0.0763 0.0759 0.0727
Orange 591-610 0.2189 0.2031 0.1987 0.1947 0.1933 0.1901
Red 610-760 0.4494 0.3965 0.3888 0.3815 0.3856 0.3805
total (400-700) 16.45 15.63 15.41 15.24 15.12 15.06
Fiber 22 - PMMA + Eosin
Inside, UP + Lurol Oil mW/cm2 at 5 cm
Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 14.39 14.36 14.33 14.28 14.27 4.39 95.7%
Fluoresc. 519-760 0.63 0.63 0.62 0.61 0.60 0.19 4.2%
total 400-760 15.01809 14.9848 14.95077 14.89236 14.87711 4.58 99.9%
% fluorescence 4.2% 4.2% 4.1% 4.1% 4.1% 0.04 4.2%
purple (400)-450  9.6369 9.5602 9.5019 9.4261 9.3807 2.97 64.9%
Blue 450-500 4.7496 4.7990 4.8327 4.8559 4.8920 1.41 30.8%
Green 500-570 0.0000 0.0000 0.0000 0.0000 0.0000 0.00 0.0%
Yellow 570-591 0.0720 0.0703 0.0683 0.0664 0.0642 0.02 0.5%
Orange 591-610 0.1884 0.1865 0.1828 0.1805 0.1789 0.06 1.3%
Red 610-760 0.3825 0.3799 0.3760 0.3743 0.3721 0.12 2.5%
total (400-700) 15.03 15.00 14.96 14.90 14.89 4.58 100.0%
TABLE 28
Fiber 23 - PMMA + Eosin Inside, Bicarbonate + Lurol Oil Outside
Fiber 23 - PMMA + Eosin
Inside, Bicarbonate + Lurol mW/cm2 at 5 cm
Oil Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 13.15 13.50 13.34 13.26 13.22 13.13
Fluoresc. 519-760 0.68 0.64 0.63 0.62 0.61 0.61
total 400-760 13.83246 14.1425 13.97107 13.88749 13.82635 13.73764
% fluorescence 4.9% 4.5% 4.5% 4.5% 4.4% 4.4%
purple (400)-450  9.3441 9.4130 9.2256 9.1099 9.0173 8.9034
Blue 450-500 3.8100 4.0877 4.1181 4.1541 4.1999 4.2260
Green 500-570 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000
Yellow 570-591 0.0804 0.0695 0.0664 0.0646 0.0623 0.0606
Orange 591-610 0.2044 0.1888 0.1839 0.1819 0.1782 0.1759
Red 610-760 0.4057 0.3948 0.3881 0.3880 0.3795 0.3824
total (400-700) 13.84 14.15 13.98 13.90 13.84 13.75
Fiber 23 - PMMA + Eosin
Inside, Bicarbonate + Lurol mW/cm2 at 5 cm
Oil Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 12.89 12.80 12.69 12.59 12.51 3.92 95.4%
Fluoresc. 519-760 0.61 0.60 0.60 0.59 0.59 0.19 4.5%
total 400-760 13.49795 13.40275 13.28483 13.18373 13.09997 4.10 99.9%
% fluorescence 4.5% 4.5% 4.5% 4.5% 4.5% 0.05 4.5%
purple (400)-450  8.7126 8.6168 8.5063 8.4182 8.3422 2.68 65.2%
Blue 450-500 4.1747 4.1828 4.1792 4.1748 4.1704 1.24 30.2%
Green 500-570 0.0000 0.0000 0.0000 0.0000 0.0000 0.00 0.0%
Yellow 570-591 0.0604 0.0597 0.0591 0.0576 0.0565 0.02 0.5%
Orange 591-610 0.1761 0.1742 0.1728 0.1704 0.1683 0.05 1.3%
Red 610-760 0.3847 0.3798 0.3780 0.3732 0.3729 0.12 2.8%
total (400-700) 13.51 13.41 13.30 13.19 13.11 4.11 100.0%
TABLE 29
Fiber 24 - PMMA + Eosin Inside, Eosin + Lurol Oil Outside
Fiber 24 - PMMA + Eosin
Inside, Eosin + Lurol Oil mW/cm2 at 5 cm
Outside 0 0.5 min 1 min 1.5 min 2 min 2.5 min
Lamp 400-518 13.69 13.11 13.01 12.84 12.64 12.72
Fluoresc. 519-760 0.49 0.47 0.46 0.45 0.44 0.44
total 400-760 14.1806 13.57408 13.46488 13.29157 13.08745 13.16511
% fluorescence 3.5% 3.4% 3.4% 3.4% 3.4% 3.4%
purple (400)-450  9.6291 9.0682 8.9211 8.7398 8.5535 8.5459
Blue 450-500 4.0575 4.0408 4.0850 4.1040 4.0914 4.1746
Green 500-570 0.0000 0.0000 0.0000 0.0000 0.0000 0.0000
Yellow 570-591 0.0456 0.0374 0.0362 0.0350 0.0332 0.0325
Orange 591-610 0.1404 0.1264 0.1243 0.1215 0.1201 0.1197
Red 610-760 0.3167 0.3091 0.3061 0.2989 0.2969 0.3000
total (400-700) 14.19 13.58 13.47 13.30 13.10 13.17
Fiber 24 - PMMA + Eosin
Inside, Eosin + Lurol Oil mW/cm2 at 5 cm
Outside 3 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 12.91 12.48 12.70 12.93 13.08 3.87 96.6%
Fluoresc. 519-760 0.44 0.43 0.43 0.43 0.43 0.13 3.4%
total 400-760 13.35073 12.91267 13.13371 13.35688 13.50934 4.01 99.9%
% fluorescence 3.3% 3.4% 3.3% 3.2% 3.2% 0.03 3.4%
purple (400)-450  8.6049 8.2940 8.3781 8.4711 8.5391 2.62 65.3%
Blue 450-500 4.3091 4.1839 4.3231 4.4581 4.5427 1.25 31.3%
Green 500-570 0.0000 0.0000 0.0000 0.0000 0.0000 0.00 0.0%
Yellow 570-591 0.0312 0.0309 0.0308 0.0294 0.0296 0.01 0.3%
Orange 591-610 0.1158 0.1154 0.1157 0.1133 0.1139 0.04 0.9%
Red 610-760 0.2972 0.2959 0.2933 0.2922 0.2913 0.09 2.3%
total (400-700) 13.36 12.92 13.14 13.36 13.52 4.01 100.0%
TABLE 30
Color Breakdown for fluorescence emission of nylon fibers
Color Fiber
12 Fiber 13 Fiber 14 Fiber 15
Purple 2.51 2.25 2.47 2.44
Blue 1.21 1.05 1.07 1.07
Green 0.45 0.46 0.41 0.27
Yellow 0.45 0.45 0.38 0.42
Orange 0.30 0.30 0.25 0.32
Red 0.41 0.42 0.35 0.42
TABLE 31
Color Breakdown for fluorescence emission of PBT fibers
Color Fiber
16 Fiber 17 Fiber 18 Fiber 19 Fiber 20
Purple 12.13 0.47 0.17 0.19 0.78
Blue 8.37 0.22 0.09 0.10 0.44
Green 0.05 0.02 0.01 0.01 0.02
Yellow 0.00 0.14 0.10 0.10 0.12
Orange 0.00 0.19 0.13 0.13 0.17
Red 0.00 0.44 0.32 0.33 0.41
TABLE 32
Color Breakdown for fluorescence emission of PMMA fibers
Color Fiber
21 Fiber 22 Fiber 23 Fiber 24
Purple 2.21 2.97 2.68 2.62
Blue 0.78 1.41 1.24 2.25
Green 0.00 0.00 0.00 0.00
Yellow 0.03 0.02 0.02 0.01
Orange 0.06 0.06 0.05 0.04
Red 0.10 0.12 0.12 0.09
The influence of the polymer on the fluorescence emitted by the fibers was measured and compared between the various fibers prepared. The results are presented in FIG. 2D. The data shows that fibers made from polyethylene and PBT fluoresce the most.
TABLE 33
Color Breakdown for fluorescence emission of the indicated fibers
Polylactic Poly-
Color Polyethylene Acid propylene Nylon PBT PMMA
Purple 8.81 2.95 7.32 2.51 0.47 2.21
Blue 5.08 1.47 4.00 1.21 0.22 0.78
Green 0.01 0.03 0.01 0.45 0.02 0.00
Yellow 0.00 0.08 0.00 0.45 0.14 0.03
Orange 0.00 0.09 0.00 0.30 0.19 0.06
Red 0.01 0.09 0.00 0.41 0.44 0.10
Example 4 Leaching of Photoactivatable Agent Out of Photoactivatable Fibers
The purpose of this experiment was to determine whether the polymer has an effect on the leaching of the photoactivatable agent out of the photoactivatable fibers. Leaching was measured by placing 0.1 g of fiber in 10 ml of water for 1 day following which the water was assessed for the presence of photoactivatable agent. FIG. 3 shows the leaching of Eosin out of the photoactivatable fibers as defined in Example 3. The detection limit for samples in FIG. 4 was 0.0095 μg/ml. Table 34 outlines the data obtained during this experiment. The data presented in Table 34 and illustrated in FIG. 3 demonstrates that photoactivatable fibers made from polyethylene and photoactivatable fibers made from PBT present the least leaching of Eosin amongst the polymers tested. The data also show that compounding the photoactivatable agent with the polymer of the fiber leads to substantially no leaching of the photoactivatable agent out of the photoactivatable fiber.
TABLE 34
Leaching of Eosin out of
photoactivatable fibers as defined in Example 3
Concentration
Photoactivatable in solution %
Fiber Photoactivatable agent (ppm) leaching
1 Compounded 0.103 0.454
2 Compounded 0.116 0.510
3 Compounded 0.154 0.676
4 Compounded and coated 0.351 1.544
5 Compounded 0.046 0.102
6 Compounded 0.046 0.102
7 Compounded 0.041 0.090
8 Compounded 0.048 0.211
9 Compounded 0.041 0.183
10 Compounded 0.049 0.214
11 Compounded and coated 0.546 2.404
12 Compounded 0.022 0.099
13 Compounded 0.017 0.074
14 Compounded 0.065 0.286
15 Compounded and coated 0.899 3.957
17 Compounded BDL N/A
18 Compounded BDL N/A
19 Compounded BDL N/A
20 Compounded and coated 0.184337 0.4055414
21 Compounded 0.102 0.224
22 Compounded 0.118 0.261
23 Compounded 0.184 0.405
24 Compounded and coated 1.495 3.290
Example 5 Effect of Varying Lamp Height on Fluorescence Emitted by Photoactivatable Fibers
The purpose of this experiment was to determine the effect of varying the blue lamp height on fluorescence emission of the photoactivatable fibers. Measurements are presented in Tables 35-38 below.
TABLE 35
Blue lamp output
Height Energy Change Percent
(cm) (J/cm2) in height Change in energy Energy increase
5 30.43
3.75 39.15 −1.25 8.72 22.28
2.5 49.78 −1.25 10.63 21.35
TABLE 36
Influence of height of blue lamp from nylon photoactivatable fibers on fluorescence emission
0-5 minutes 5-10 minutes
Percent Percent
Height Energy Change Change in Energy Energy Change Change in Energy
(cm) (J/cm2) in height energy increase (J/cm2) in height energy increase
5 1.59 1.02
3.75 1.64 −1.25 0.05 3.19 0.96 −1.25 −0.06 −6.60
2.5 1.90 −1.25 0.26 15.66 1.09 −1.25 0.13 13.83
TABLE 37
Influence of height of blue lamp from PBT photoactivatable fibers on fluorescence emission
0-5 minutes 5-10 minutes
Percent Percent
Height Energy Change Change in Energy Energy Change Change in Energy
(cm) (J/cm2) in height energy increase (J/cm2) in height energy increase
5 0.77 0.67
2.5 1.04 −2.50 0.28 26.54 0.80 −2.50 0.13 19.88
TABLE 38
Influence of height of blue lamp from PLA photoactivatable fibers on fluorescence emission
0-5 minutes 5-10 minutes
Percent Percent
Height Energy Change Change in Energy Energy Change Change in Energy
(cm) (J/cm2) in height energy increase (J/cm2) in height energy increase
5 0.28 0.24
2.5 0.39 −2.50 0.11 27.25 0.25 −2.50 0.01 2.83
As the blue lamp height decreases, the fluorescence and the energy produced by the photoactivatable fiber increases in a non-linear fashion. For nylon fibers, the effect is seen in the first five minutes. The fluorescence and energy are 12.95 mW/cm2 for fluorescence and 1.90 J/cm2 for energy. After five minutes, it was observed that the fluorescence and the energy were similar. For PBT fibers, decreasing the lamp height increases both fluorescence and energy. However, photobleaching occurs more rapidly. For PLA fibers, decreasing the lamp height increases fluorescence at first. Photobleaching occurs at a rate such that after 7 minutes the fluorescence is lower when the lamp is closer.
Example 6 Effect of Addition of a Lubricant on the Fluorescence Emitted from Eosin Y
The purpose of this experiment was to assess if addition of a lubricant affects the emission of fluorescence of a solution of Eosin Y. When lurol oil is added to a solution of Eosin Y in water the solution immediately turns from an orange color to a pink color. It also may get slightly bubbly. A quick check of the solution with lurol oil shows that the solution is one layer, completely miscible, with no visible precipitate. The effect of lurol oil was compared by adding 320 μL to a 2 mL solution of 109 μg/g Eosin Y. The no lurol oil solution had 320 μL. of water added. The fluorescence of these two solutions was measured to determine if the lurol oil had any effect (FIG. 4). The results indicated that the lurol oil has an effect of the Eosin Y solution, as the lurol oil solution was almost twice as fluorescent and barely photodegraded. Also, the fluorescence of the lurol oil is red shifted, such that some yellow and orange are observed. Under the blue lamp the lurol oil solution looks almost orange, while the solution without lurol oil was green.
Example 7 Effect of Addition of a Lubricant on the Fluorescence Emission of Photoactivatable Fibers
The presence of a lubricant was shown to have an effect on the doped fibers and their fluorescence. In the case of low concentrations of chromophore it can slightly red shift, and reduces bleaching time considerably. In higher concentrations of chromophore it red shifts, as well as increase fluorescence. The most effect seems to be around 10 g/L of lurol oil. Initially the fluorescence of Eosin Y doped fibers was 0.01 (FIG. 5A), but with the lurol oil added the fluorescence is boosted to 0.7. A comparison was done of Eosin Y and Fluorescein at the same concentration with lurol oil added. It would appear that while they start out similarly in fluorescence, the fluorescein photo-degrades faster (FIG. 5B).
Example 8 Preparation of Photoactivatable Fibers with Multiple Layers of Photoactivatable Agents
The purpose of this experiment was to determine if adding more than one layer of photoactivatable agents onto the polymeric fibers affect the emission of fluorescence. For this, the following photoactivatable fibers were prepared. The polypropylene polymer was compounded with the photoactivatable agent (Eosin Y:fluorescein) at around 0.8-1.0% w/w and the polymer was then hardened and cut into small pieces. This polymer was processed into the hopper and it was extruded into a fiber at specific micron sizes (FIG. 6A: 31 microns) (FIG. 6B: 93 microns). As it was exiting from the machine head, it was sprayed with a composition of lurol oil alone, or with a composition of lurol oil and photoactivatable agent, or with a composition of lurol oil and urea peroxide, or with a composition of lurol oil and sodium bicarbonate.
The amount of fluorophore is determinant for overall fluorescence of the photoactivatable fibers. As the layer level increases the overall fluorescence also increases. The increase is not linear, and doubling the fiber content does not double the fluorescence. It is clear however that 6 layers out preforms both 4 and 2 layers of the same material.
Example 9 Influence of with Multiple Layers of Photoactivatable Agents on Fluorescence Emission
When the chromophore is situated on the surface of the polymeric fibers, increasing the number of layers also increases the fluorescence of the polymeric fiber. When the chromophore is on the inside, the opposite happens, increasing the number of layers decreases overall fluorescence. The photoactivatable fibers were prepared as described in Example 8. Photobleaching occurs more rapidly when the chromophore is on the inside (FIG. 7). When comparing the 4 layer 50 g/L Eosin Y Outer from Trial 2 and 4 layer 0.5% Eosin Y Inner from Trial 3, the rate of photobleaching is faster when Eosin Y is compounded with nylon. Nylon trial 3 was more successful than nylon trial 2. With less chromophore within the fiber and with less layers, it fluoresced more than with the chromophore coating the fiber. However, photobleaching occurs at a much faster rate. A difference of 2 mW/cm2 is observed between them after 10 minutes.
TABLE 39
Color breakdown of the fluorescence emitted
Trial 3 Trial 3
Trial 2 Trial 2 Trial 2 2 layers 4 layers
4 layers 2 layers 4 layers 0.5% Eosin Inner 0.5% Eosin Inner
Color
50 g/L Eosin Y 50 g/L E:F 50 g/L E:F Lurol Oil Outer Lurol Oil Outer
Purple 2.63 6.21 1.87 2.51 0.29
Blue 1.27 3.49 0.90 1.21 0.08
Green 0.22 0.32 0.31 0.45 0.21
Yellow 0.56 0.47 0.66 0.45 0.35
Orange 0.44 0.34 0.51 0.30 0.26
Red 0.50 0.27 0.60 0.41 0.41
TABLE 40
Nylon Run 1-103 microns E/F 10 g/L-4 Layers 0-5 min
Nylon Run 1-103 microns mW/cm2 at 5 cm
E/F 10 g/L-4 Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 21.47 24.99 25.79 26.31 26.83 27.22 27.44
Fluoresc. 519-760 3.12 5.17 4.70 4.34 4.03 3.85 3.68
total 400-760 24.58338 30.15935 30.49297 30.65144 30.85972 31.07188 31.11921
% fluorescence 12.7% 17.1% 15.4% 14.2% 13.1% 12.4% 11.8%
purple (400)-450   14.2387 15.8609 16.1645 16.2767 16.4031 16.5001 16.5381
Blue 450-500 7.2285 8.9835 9.4986 9.9158 10.3133 10.6121 10.7933
Green 500-570 1.2302 2.1414 1.9567 1.7172 1.5957 1.5291 1.4669
Yellow 570-591 1.1034 1.4359 1.3037 1.1519 1.0679 1.0119 0.9749
Orange 591-610 0.6207 0.8740 0.7901 0.7554 0.7005 0.6657 0.6391
Red 610-760 0.1814 0.8965 0.8084 0.8645 0.8071 0.7795 0.7324
total (400-700) 24.60 30.19 30.52 30.68 30.89 31.10 31.14
Nylon Run 1-103 microns mW/cm2 at 5 cm
E/F 10 g/L-4 Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 27.69 27.95 28.21 28.36 7.92 87.0%
Fluoresc. 519-760 3.53 3.49 3.32 3.17 1.18 12.9%
total 400-760 31.21439 31.43356 31.52938 31.53128 9.09 99.9%
% fluorescence 11.3% 11.1% 10.5% 10.0% 0.13 12.9%
purple (400)-450   16.5781 16.6734 16.7323 16.7269 4.86 53.4%
Blue 450-500 11.0066 11.1705 11.3788 11.5401 3.03 33.3%
Green 500-570 1.4155 1.3995 1.3350 1.2853 0.47 5.2%
Yellow 570-591 0.9367 0.9109 0.8637 0.8309 0.32 3.5%
Orange 591-610 0.6134 0.5987 0.5662 0.5442 0.20 2.2%
Red 610-760 0.6883 0.7045 0.6760 0.6255 0.21 2.4%
total (400-700) 31.24 31.46 31.55 31.55 9.10 100.0%
TABLE 41
Nylon Run 1-103 microns E/F 20 g/L-4 Layers 0-5 min
Nylon Run 1-103 microns mW/cm2 at 5 cm
E/F 10 g/L-4 Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 19.40 21.27 22.67 22.77 23.13 23.67 24.11
Fluoresc. 519-760 7.72 6.40 5.79 5.81 5.63 5.45 5.18
total 400-760 27.12141 27.67375 28.45756 28.58048 28.76461 29.12852 29.29128
% fluorescence 28.5% 23.1% 20.4% 20.3% 19.6% 18.7% 17.7%
purple (400)-450   12.6847 13.4080 14.0379 14.1004 14.2567 14.5022 14.6514
Blue 450-500 6.6370 7.7965 8.5687 8.6018 8.8139 9.1072 9.4021
Green 500-570 2.2366 1.8797 1.6972 1.7004 1.6593 1.6050 1.5366
Yellow 570-591 2.4298 1.9811 1.7822 1.7786 1.7244 1.6595 1.5891
Orange 591-610 1.5572 1.2861 1.1626 1.1594 1.1250 1.0824 1.0351
Red 610-760 1.6340 1.3711 1.2534 1.2832 1.2280 1.2135 1.1167
total (400-700) 27.18 27.72 28.50 28.62 28.81 29.17 29.33
Nylon Run 1-103 microns mW/cm2 at 5 cm
E/F 10 g/L-4 Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 24.51 24.92 25.30 25.57 6.95 80.2%
Fluoresc. 519-760 5.03 4.87 4.75 4.66 1.70 19.6%
total 400-760 29.53686 29.79402 30.04862 30.22247 8.65 99.9%
% fluorescence 17.0% 16.4% 15.8% 15.4% 0.20 19.6%
purple (400)-450   14.8214 14.9772 15.1395 15.2521 4.28 49.4%
Blue 450-500 9.6311 9.8833 10.0927 10.2565 2.66 30.7%
Green 500-570 1.4934 1.4625 1.4331 1.4059 0.50 5.8%
Yellow 570-591 1.5402 1.4879 1.4429 1.4163 0.52 6.0%
Orange 591-610 1.0043 0.9687 0.9394 0.9180 0.34 3.9%
Red 610-760 1.0842 1.0517 1.0368 1.0080 0.37 4.2%
total (400-700) 29.57 29.83 30.08 30.26 8.66 100.0%
TABLE 42
Nylon Run 7 Fluorescein 35 g/L-4 Layers 0-5 min
Nylon Run 7 Fluorescein mW/cm2 at 5 cm
35 g/L-4 Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 10.68 11.92 12.89 13.63 14.33 14.95 15.60
Fluoresc. 519-760 10.30 9.13 8.49 8.01 7.59 7.16 6.83
total 400-760 20.98009 21.05839 21.38843 21.64094 21.92016 22.11076 22.42923
% fluorescence 49.1% 43.4% 39.7% 37.0% 34.6% 32.4% 30.4%
purple (400)-450   6.7401 7.2458 7.6859 8.0035 8.3020 8.5583 8.8489
Blue 450-500 3.5037 4.2174 4.7250 5.1256 5.5065 5.8505 6.2007
Green 500-570 6.4483 5.8166 5.4777 5.2332 5.0226 4.8153 4.6339
Yellow 570-591 1.8820 1.6354 1.4990 1.3971 1.3096 1.2236 1.1540
Orange 591-610 1.0807 0.9469 0.8767 0.8197 0.7732 0.7270 0.6870
Red 610-760 1.3665 1.2324 1.1575 1.0932 1.0361 0.9634 0.9312
total (400-700) 21.02 21.09 21.42 21.67 21.95 22.14 22.46
Nylon Run 7 Fluorescein mW/cm2 at 5 cm
35 g/L-4 Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 16.21 16.71 17.21 17.61 4.32 65.4%
Fluoresc. 519-760 6.42 6.17 5.88 5.65 2.28 34.5%
total 400-760 22.63264 22.88359 23.0868 23.25756 6.60 99.9%
% fluorescence 28.4% 27.0% 25.5% 24.3% 0.35 34.5%
purple (400)-450   9.0966 9.3179 9.5100 9.6820 2.50 37.8%
Blue 450-500 6.5468 6.8184 7.1173 7.3422 1.67 25.2%
Green 500-570 4.4415 4.3017 4.1459 4.0237 1.51 22.8%
Yellow 570-591 1.0778 1.0244 0.9718 0.9246 0.40 6.0%
Orange 591-610 0.6431 0.6127 0.5811 0.5564 0.23 3.5%
Red 610-760 0.8515 0.8318 0.7831 0.7505 0.31 4.6%
total (400-700) 22.66 22.91 23.11 23.28 6.61 100.0%
TABLE 43
Nylon Run 9C-103 microns E/F 30/7.5/7.5-4 Layers 0-5 min
Nylon Run 9C-103 microns
E/F 30/7.5/7.5-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 20.92 21.07 21.36 21.56 21.77 21.82 21.92
Fluoresc. 519-760 1.54 1.41 1.39 1.36 1.36 1.34 1.34
total 400-760 22.45942 22.48255 22.74403 22.9241 23.12528 23.16169 23.26146
% fluorescence 6.9% 6.3% 6.1% 5.9% 5.9% 5.8% 5.8%
purple (400)-450   14.2461 14.0180 14.0744 14.0780 14.0611 14.0484 14.0565
Blue 450-500 6.6739 7.0542 7.2817 7.4833 7.7090 7.7720 7.8656
Green 500-570 0.0700 0.0640 0.0625 0.0652 0.0690 0.0682 0.0698
Yellow 570-591 0.3880 0.3600 0.3510 0.3480 0.3480 0.3455 0.3465
Orange 591-610 0.5250 0.4839 0.4742 0.4657 0.4584 0.4548 0.4544
Red 610-760 0.5830 0.5270 0.5243 0.5075 0.5028 0.4956 0.4916
total (400-700) 22.49 22.51 22.77 22.95 23.15 23.18 23.28
Nylon Run 9C-103 microns
E/F 30/7.5/7.5-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 22.02 22.17 22.33 22.48 6.51 94.0%
Fluoresc. 519-760 1.33 1.29 1.31 1.30 0.41 5.9%
total 400-760 23.35004 23.46191 23.64257 23.78278 6.92 99.9%
% fluorescence 5.7% 5.5% 5.5% 5.5% 0.06 5.9%
purple (400)-450   14.0161 14.0168 14.0343 14.0449 4.22 60.9%
Blue 450-500 8.0056 8.1532 8.3002 8.4356 2.29 33.1%
Green 500-570 0.0715 0.0696 0.0761 0.0801 0.02 0.3%
Yellow 570-591 0.3454 0.3405 0.3456 0.3501 0.11 1.5%
Orange 591-610 0.4491 0.4407 0.4421 0.4408 0.14 2.0%
Red 610-760 0.4848 0.4631 0.4663 0.4531 0.15 2.2%
total (400-700) 23.37 23.48 23.66 23.80 6.93 100.0%
TABLE 44
Polypropylene Run 10 Fluorescein 35 g/L-4 Layers 0-5 min
Polypropylene Run 10
Fluorescein 35 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 34.75 35.18 35.26 35.19 35.26 35.20 35.11
Fluoresc. 519-760 0.58 0.63 0.60 0.46 0.45 0.41 0.38
total 400-760 35.32948 35.80934 35.85791 35.65735 35.70358 35.60884 35.48748
% fluorescence 1.6% 1.8% 1.7% 1.3% 1.3% 1.1% 1.1%
purple (400)-450  21.5860 21.4518 21.3402 20.8147 20.7911 20.6313 20.4316
Blue 450-500 13.0286 13.5733 13.7616 14.2367 14.3212 14.4363 14.5448
Green 500-570 0.5551 0.5656 0.5458 0.4488 0.4390 0.4082 0.3877
Yellow 570-591 0.1004 0.1011 0.0941 0.0763 0.0704 0.0666 0.0622
Orange 591-610 0.0477 0.0609 0.0577 0.0443 0.0441 0.0397 0.0369
Red 610-760 0.0132 0.0590 0.0608 0.0382 0.0396 0.0282 0.0258
total (400-700) 35.33 35.81 35.86 35.66 35.71 35.61 35.49
Polypropylene Run 10
Fluorescein 35 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 35.10 34.95 34.88 34.86 10.53 98.7%
Fluoresc. 519-760 0.37 0.31 0.30 0.29 0.13 1.3%
total 400-760 35.47158 35.25517 35.18271 35.15384 10.66 100.0%
% fluorescence 1.0% 0.9% 0.9% 0.8% 0.01 1.3%
purple (400)-450  20.3492 20.1362 20.0194 19.9225 6.23 58.4%
Blue 450-500 14.6194 14.6803 14.7432 14.8173 4.26 39.9%
Green 500-570 0.3818 0.3440 0.3258 0.3198 0.13 1.2%
Yellow 570-591 0.0591 0.0486 0.0467 0.0454 0.02 0.2%
Orange 591-610 0.0364 0.0289 0.0289 0.0273 0.01 0.1%
Red 610-760 0.0271 0.0182 0.0197 0.0226 0.01 0.1%
total (400-700) 35.47 35.26 35.18 35.15 10.66 100.0%
TABLE 45
Polypropylene Run 12 Eosin y 25 g/L-4 Layers 0-5 min
Polypropylene Run 12
Eosin y 25 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 20.35 20.29 20.27 20.23 20.19 20.17 20.12
Fluoresc. 519-760 0.84 0.81 0.80 0.79 0.78 0.78 0.77
total 400-760 21.1856 21.09802 21.06914 21.02316 20.96994 20.94642 20.8899
% fluorescence 4.0% 3.8% 3.8% 3.8% 3.7% 3.7% 3.7%
purple (400)-450  13.7608 13.4286 13.2875 13.1247 12.9928 12.8698 12.7363
Blue 450-500 6.5846 6.8630 6.9810 7.1075 7.1948 7.2987 7.3816
Green 500-570 0.1434 0.1414 0.1371 0.1356 0.1310 0.1287 0.1287
Yellow 570-591 0.2980 0.2976 0.2957 0.2925 0.2902 0.2867 0.2854
Orange 591-610 0.2576 0.2460 0.2432 0.2400 0.2387 0.2383 0.2366
Red 610-760 0.1509 0.1306 0.1338 0.1319 0.1314 0.1333 0.1302
total (400-700) 21.20 21.11 21.08 21.03 20.98 20.96 20.90
Polypropylene Run 12
Eosin y 25 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 20.13 20.09 20.11 20.09 6.06 96.2%
Fluoresc. 519-760 0.77 0.76 0.76 0.76 0.24 3.7%
total 400-760 20.89411 20.85018 20.8722 20.85232 6.29 100.0%
% fluorescence 3.7% 3.6% 3.7% 3.7% 0.04 3.7%
purple (400)-450  12.6547 12.5548 12.4838 12.4130 3.90 61.9%
Blue 450-500 7.4711 7.5354 7.6239 7.6759 2.16 34.3%
Green 500-570 0.1258 0.1257 0.1261 0.1258 0.04 0.6%
Yellow 570-591 0.2838 0.2835 0.2843 0.2841 0.09 1.4%
Orange 591-610 0.2356 0.2336 0.2341 0.2328 0.07 1.1%
Red 610-760 0.1320 0.1260 0.1290 0.1295 0.04 0.6%
total (400-700) 20.90 20.86 20.88 20.86 6.30 100.0%
TABLE 46
Polypropylene Run 15B E/F/RB 20/5/5 (g/L)-4 Layers 0-5 min
Polypropylene Run 15B
E/F/RB 20/5/5 (g/L)-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 25.41 25.50 25.59 25.65 25.72 25.76 25.80
Fluoresc. 519-760 0.83 0.78 0.76 0.74 0.73 0.72 0.71
total 400-760 26.23634 26.28132 26.34717 26.39618 26.44999 26.4881 26.5104
% fluorescence 3.2% 3.0% 2.9% 2.8% 2.8% 2.7% 2.7%
purple (400)-450  16.5085 16.3661 16.2357 16.1308 16.0312 15.9348 15.8525
Blue 450-500 8.8967 9.1325 9.3518 9.5209 9.6896 9.8291 9.9452
Green 500-570 0.0424 0.0335 0.0338 0.0317 0.0318 0.0339 0.0339
Yellow 570-591 0.2430 0.2265 0.2220 0.2187 0.2144 0.2158 0.2143
Orange 591-610 0.2914 0.2797 0.2711 0.2657 0.2593 0.2577 0.2525
Red 610-760 0.2676 0.2562 0.2455 0.2408 0.2358 0.2289 0.2237
total (400-700) 26.25 26.29 26.36 26.41 26.46 26.50 26.52
Polypropylene Run 15B
E/F/RB 20/5/5 (g/L)-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 25.82 25.85 25.91 25.94 7.71 97.2%
Fluoresc. 519-760 0.70 0.69 0.68 0.68 0.22 2.8%
total 400-760 26.51969 26.5395 26.5943 26.62222 7.93 100.0%
% fluorescence 2.6% 2.6% 2.6% 2.6% 0.03 2.8%
purple (400)-450  15.7523 15.7119 15.6652 15.6041 4.81 60.6%
Blue 450-500 10.0682 10.1388 10.2448 10.3347 2.90 36.6%
Green 500-570 0.0342 0.0351 0.0372 0.0380 0.01 0.1%
Yellow 570-591 0.2133 0.2104 0.2097 0.2118 0.07 0.8%
Orange 591-610 0.2497 0.2456 0.2409 0.2387 0.08 1.0%
Red 610-760 0.2135 0.2088 0.2076 0.2058 0.07 0.9%
total (400-700) 26.53 26.55 26.61 26.63 7.93 100.0%
TABLE 47
Polypropylene core with Polyethylene sheath, Fluorescein, 30 g/L-4 Layers 0-5 min
Polypropylene core with
Polyethylene sheath,
Fluorescein, 30 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 23.10 24.18 24.29 24.54 24.89 25.20 25.33
Fluoresc. 519-760 1.91 1.56 1.52 1.43 1.27 1.16 1.06
total 400-760 25.01102 25.73662 25.8135 25.97069 26.16178 26.35745 26.39481
% fluorescence 7.6% 6.0% 5.9% 5.5% 4.9% 4.4% 4.0%
purple (400)-450  14.4848 14.7578 14.8113 14.8620 14.9236 14.9942 14.9548
Blue 450-500 8.4257 9.2502 9.3024 9.5154 9.8149 10.0590 10.2412
Green 500-570 1.2588 1.0645 1.0456 0.9803 0.8771 0.8112 0.7264
Yellow 570-591 0.3698 0.3003 0.2976 0.2783 0.2503 0.2278 0.2113
Orange 591-610 0.2250 0.1784 0.1778 0.1635 0.1457 0.1334 0.1285
Red 610-760 0.2560 0.1919 0.1862 0.1777 0.1555 0.1368 0.1378
total (400-700) 25.02 25.74 25.82 25.98 26.17 26.36 26.40
Polypropylene core with
Polyethylene sheath,
Fluorescein, 30 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 25.54 25.68 25.76 25.83 7.46 95.1%
Fluoresc. 519-760 0.99 0.96 0.88 0.84 0.38 4.9%
total 400-760 26.52577 26.64275 26.64462 26.66904 7.84 100.0%
% fluorescence 3.7% 3.6% 3.3% 3.1% 0.05 4.9%
purple (400)-450  14.9895 14.9871 14.9555 14.9339 4.46 56.9%
Blue 450-500 10.4189 10.5712 10.6820 10.7803 2.95 37.6%
Green 500-570 0.6795 0.6468 0.6059 0.5693 0.26 3.3%
Yellow 570-591 0.1983 0.1879 0.1763 0.1669 0.07 1.0%
Orange 591-610 0.1196 0.1159 0.1082 0.1014 0.04 0.6%
Red 610-760 0.1247 0.1385 0.1210 0.1213 0.05 0.6%
total (400-700) 26.53 26.65 26.65 26.67 7.84 100.0%
TABLE 48
Polypropylene core/Polyethylene sheath, E:F:RB, 20 g/:5 g/L:5 g/L-4 Layers 0-5 min
Polypropylene
core/Polyethylene
sheath, E:F:RB,
20 g/:5 g/L:5 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 23.53 23.65 23.69 23.72 23.77 23.77 23.83
Fluoresc. 519-760 0.98 0.94 0.89 0.87 0.85 0.83 0.82
total 400-760 24.50132 24.58279 24.58891 24.59305 24.62182 24.6087 24.65408
% fluorescence 4.0% 3.8% 3.6% 3.5% 3.4% 3.4% 3.3%
purple (400)-450  15.7772 15.6065 15.4681 15.3450 15.1697 15.0644 15.0060
Blue 450-500 7.7480 8.0411 8.2265 8.3771 8.6030 8.7102 8.8288
Green 500-570 0.0396 0.0323 0.0291 0.0276 0.0286 0.0265 0.0275
Yellow 570-591 0.2661 0.2586 0.2495 0.2456 0.2394 0.2338 0.2327
Orange 591-610 0.3425 0.3369 0.3225 0.3156 0.3047 0.3008 0.2960
Red 610-760 0.3442 0.3234 0.3087 0.2973 0.2910 0.2873 0.2772
total (400-700) 24.52 24.60 24.60 24.61 24.64 24.62 24.67
Polypropylene
core/Polyethylene
sheath, E:F:RB,
20 g/:5 g/L:5 g/L-4 mW/cm2 at 5 cm
Layers 0-5 min 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 23.87 23.92 23.96 23.99 7.13 96.5%
Fluoresc. 519-760 0.82 0.80 0.79 0.78 0.26 3.5%
total 400-760 24.69701 24.72073 24.74822 24.7711 7.39 99.9%
% fluorescence 3.3% 3.2% 3.2% 3.1% 0.03 3.5%
purple (400)-450  14.9231 14.8477 14.7970 14.7369 4.56 61.7%
Blue 450-500 8.9500 9.0729 9.1644 9.2549 2.57 34.8%
Green 500-570 0.0271 0.0281 0.0282 0.0282 0.01 0.1%
Yellow 570-591 0.2335 0.2282 0.2260 0.2240 0.07 1.0%
Orange 591-610 0.2944 0.2866 0.2829 0.2797 0.09 1.3%
Red 610-760 0.2830 0.2709 0.2632 0.2605 0.09 1.2%
total (400-700) 24.71 24.73 24.76 24.78 7.39 100.0%
TABLE 49
Royal Carolina Media, Eosin:Fluorescein, 1 layer
RoyalCarolina Media, mW/cm2 at 5 cm
Eosin:Fluorescein, 1 layer 0 0.5 min 1 min 1.5 min 2 min 2.5 min 3 min
Lamp 400-518 45.18 44.92 44.87 44.82 44.75 44.69 44.66
Fluoresc. 519-760 0.78 0.79 0.78 0.75 0.73 0.72 0.70
total 400-760 45.96064 45.70756 45.64751 45.57463 45.4783 45.41009 45.36403
% fluorescence 1.7% 1.7% 1.7% 1.7% 1.6% 1.6% 1.5%
purple (400)-450  27.0635 26.5869 26.4423 26.2921 26.1306 25.9930 25.8850
Blue 450-500 18.1148 18.3232 18.4223 18.5199 18.6103 18.6862 18.7644
Green 500-570 0.2912 0.2955 0.2929 0.2800 0.2687 0.2667 0.2642
Yellow 570-591 0.2904 0.2976 0.2912 0.2858 0.2791 0.2745 0.2699
Orange 591-610 0.1584 0.1609 0.1572 0.1555 0.1516 0.1508 0.1445
Red 610-760 0.0470 0.0485 0.0466 0.0461 0.0425 0.0436 0.0404
total (400-700) 45.97 45.71 45.65 45.58 45.48 45.41 45.37
RoyalCarolina Media, mW/cm2 at 5 cm
Eosin:Fluorescein, 1 layer 3.5 min 4 min 4.5 min 5 min J/cm2
Lamp 400-518 44.59 44.59 44.57 44.54 13.43 98.4%
Fluoresc. 519-760 0.68 0.67 0.66 0.65 0.22 1.6%
total 400-760 45.26928 45.2666 45.23608 45.19001 13.65 100.0%
% fluorescence 1.5% 1.5% 1.5% 1.4% 0.02 1.6%
purple (400)-450  25.7933 25.7023 25.6407 25.5755 7.85 57.5%
Blue 450-500 18.7845 18.8782 18.9181 18.9484 5.58 40.9%
Green 500-570 0.2519 0.2550 0.2530 0.2491 0.08 0.6%
Yellow 570-591 0.2593 0.2589 0.2526 0.2481 0.08 0.6%
Orange 591-610 0.1426 0.1381 0.1355 0.1327 0.04 0.3%
Red 610-760 0.0421 0.0382 0.0404 0.0403 0.01 0.1%
total (400-700) 45.27 45.27 45.24 45.19 13.65 100.0%
Example 10 Fluorescence Emission of Re-Dipped Photoactivatable Fibers
A solution of Eosin Y in water was prepared at a concentration of 0.1 g/L, and two polypropylene fibers were dipped in the solution to dope them with chromophore. They were then examined for their fluorescence as seen on DAY 1 to determine how well they retain their fluorescence over time as well as if dipped in water how much chromophore is retained. From this experiment, it can be seen that the tips of the fibers retain fluorescence after 3 days.
FIGS. 8A and 8B show the fluorescence emission under blue lamp after one day wherein the fibers were not emerged in water. FIGS. 8C and 8D show the fluorescence emission under blue lamp after three days wherein the fibers were not emerged in water. FIGS. 8E and 8F show the fluorescence emission under blue lamp after three days emerged in water.
Example 11 Qualitative Analysis of Dental Fiber Doping
Commercially available dental fibers were dipped into solutions of Eosin Y (300 g/L, 200 g/L, 100 g/L, 50 g/L, 10 g/L, 1 g/L, or 0.1 g/L) for 10 seconds. The fibers were taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively. The 300-100 g/L Eosin Y solutions showed little fluorescence, while the 50 g/L Eosin Y solution showed fluorescence. A significant increase in fluorescence was observed when the 10 g/L Eosin Y solution was used.
Dental fibers were dipped into solutions of fluorescein (50 g/L, 10 g/L, 1 g/L, 0.1 g/L) for 10 seconds. The fibers were then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively. The 50 g/L fluorescein solution showed fluorescence.
Dental fibers were dipped into solutions of fluorescein:Eosin Y 1:1 (50 g/L, 10 g/L, 1 g/L, 0.1 g/L total chromophore) solution for 10 seconds again. The fibers were then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively. The 50 g/L fluorescein:Eosin Y 1:1 solution showed little fluorescence. A significant increase in fluorescence was observed when the 10 g/L fluorescein:Eosin Y 1:1 solution was used.
FIGS. 9A-9P illustrate pictures of the fluorescence emission under blue lamp of fibers dipped in a solution of photoactivatable agents, i.e., commercial dental fibers in Eosin Y 50 g/L (FIGS. 9A-9B); commercial dental fibers in Eosin Y 0.1 g/L (FIGS. 9C-9D); commercial dental fibers in fluorescein 50 g/L (FIGS. 9E-19F), commercial dental fibers in fluorescein 0.1 g/L (FIGS. 9G-9H), commercial dental fibers in fluorescein:Eosin Y 50 g/L (FIG. 9I-9J), commercial dental fibers in fluorescein:Eosin Y 0.1 g/L (FIGS. 9K-9L), polypropylene fibers in fluorescein 50 g/L (FIGS. 9M-9N), polypropylene fibers in fluorescein 0.1 g/L (FIGS. 9O-9P).
Polypropylene fibers were dipped in solutions of fluorescein (50 g/L, 10 g/L, 1 g/L, 0.1 g/L total chromophore) for 10 seconds, then taken out and observed for color, then put under a blue lamp and the fluorescence was observed qualitatively. The 50 g/L fluorescein solution showed little fluorescence. An increase in fluorescence was observed when the 10 g/L fluorescein solution was used.
Example 12 Preparation of Photoactivatable Fabric
The polypropylene fiber used in the preparation of the photoactivatable fabric was acquired from Midwest Filtration (West Chester Township, Ohio, U.S.). The fabric tested was composed of polypropylene at densities ranging from 0.45 oz/yd2 to 2.50 oz/yd2. It was observed that the polypropylene fabric at a density of 2.00 oz/yd2 absorbs a significant amount of chromophore, while blocking less light than higher thicknesses (data not shown). A piece of the fabric was dipped in a small chromophore bath without Lurol oil PP-3771 while another piece of the fabric was dipped in a small chromophore bath comprising Lurol oil PP-3771. The dipped fabrics were then roll dried and heated in an oven. The process for the preparation of photoactivatable fabric is illustrated in FIG. 10.
Example 13 Preparation of a Photoactivatable Article of Manufacture
An article of manufacture comprising a photoactivatable fabric is envisioned. In particular, the article of manufacture is a suit made of a fabric comprising fibers (FIG. 11A). In some instances, the fibers entering the composition of the fabric may be made of a virgin polymer, that is to say a polymer that does not comprise photoactivatable agent. In some other instances, the fibers entering into the composition of the fabric may be made of photoactivatable fibers which comprise photoactivatable agents. In the instances where the fabric comprises fibers made of virgin polymer, the fabric or the article of manufacture made with such fabric may be coated, dipped or sprayed with a photoactivatable agent composition so as to deposit photoactivatable agents onto the fabric and into the interstices created between the fibers of the fabric. A composition of lubricant may also be laid onto the fabric so as to facilitate the insertion of the photoactivatable agents into the interstices created between the fibers of the fabric. In this particular example the article of manufacture is a suit which is to be worn by a subject in need of phototherapy (FIG. 11A). The photoactivatable fibers that are preferred for entering into the fabrication of the suit comprise nylon and polyethylene which comprise one or more photoactivatable agent. The resulting article of manufacture (e.g., a suit-like garment) is then photoactivated under light while being worn by the subject in need of phototherapy.
A suit-like garment was prepared by associating two photoactivatable fabrics having the following composition:
    • (1) Photoactivatable fabric #1 was made from polypropylene fibers. The resulting fabric was dipped in the composition of 0.50 g/L Eosin Y+Luroil oil.
    • (2) Photoactivatable fabric #2 was made from polypropylene fibers. The resulting fabric was dipped in the composition of 0.25 g/L Eosin Y+0.25 g/L Fluorescein+Luroil oil.
The juxtaposed photoactivatable fabrics were tailored into the suit-like garment illustrated in FIG. 11B. The two fabrics may be joined, stitched, glued, attached, fused, sewed, or bonded or the like, and thereafter tailored accordingly.
Example 14 Cytokine and Growth Factor Modulations Using Photoactivatable Fabrics
The purpose of this experiment was to assess the effect of the photoactivatable fibers of the present disclosure on secretion of cytokines and growth factors. To this end, a blue lamp (129.53 mW/cm2) was placed either on top or on the bottom of human dermal fibroblasts (passage #3 (70,000 cells/well) sample stage at 5 cm. Photoactivatable fabrics as identified in Table 50 below were wrapped around the custom made plastic frame (1-3 turn). Slides were filled with ˜1-1.4 ml of PBS and were placed on the stage directly over the fibers. Illumination carried out from bottom to top. Cells were illuminated for 13-15 J/cm2 for most of the fibers and media or for 5 J/cm2. Cells were then incubated for 24 hours in normal media/IFNg and the supernatant was collected and stored at −80° C. Antibody array assay carried out on the collected supernatant and the expression level of cytokines and growth factors were analyzed and normalizing to IFNg stimulated cells. The results presented in Table 51 are based on at least 50% difference in the expression level compared to non-treated control only.
TABLE 50
Composition of photoactivatable fibers/fabrics
Photoactivatable
Fiber/Fabric Composition
36 Fabric 1 - polypropylene fibers (blank -
no photoactivatable agent)
37 Fabric 2: polypropylene fibers + Eosin Y
38 Fabric 3: polypropylene fibers + Eosin
y and fluorescein
39 Fabric 1 + 1 (2 layers)
40 Fabric 2 + 3 (2 layers)
TABLE 51
Biological effect of Photoactivatable fabrics
Sample
Fabric 1 (Blank) Fabric 2 (E) Fabric 3 (E/F) Fabric 2 + 3 (E + E/F)
Photonic evaluation
P = 10.11, B = 6.70, P = 7.41, B = 4.37, P = 6.69, B = 4.25, P = 5.30, B = 2.86,
G = 0.04, Y = 0.00, G = 0.09, Y = 0.16, G = 0.13, Y = 0.15, G = 0.14, Y = 0.26,
O = 0.00, R = 0.00 O = 0.11, R = 0.05 O = 0.09, R = 0.03 O = 0.20, R = 0.10
Dose
15 J/cm2 15 J/cm2 15 J/cm2 15 J/cm2
Modulations
Cytokines, IL-6, GM- GM-SCF, G-SCF, I- ANG
Chemokines CSF, IL-2, IL- 309, IL-
and Growth MCP-2 13, GROα, 15, IL-7,
factors MCP-2, MDC,
MCP-3, TGFβ1,
ANG GROα,
IGF-1
P = purple,
B = blue,
G = green,
Y = yellow,
O = orange,
R = red
The results represented above are from at least two independent experiments for each media.
The results suggest that the illumination of media 2 (Eosin) and media 3 (Eosin/Fluorescein) combined (layered) may have positive impacts on down regulation of 1-309, IL-15, IL-7, MDC, TGFβ1, GROα and IGF-1. These cytokines and chemokines are involved in conditions such as contact allergic dermatitis (1-309, IL-7), psoriasis (GROα, IL-15, IGF-1), atopic dermatitis (MDC), and scarring (TGFβ1). However, these pathologies are complex and usually modulation of more proteins would be preferable.
Variations and modifications will occur to those of skill in the art after reviewing this disclosure. The disclosed features may be implemented, in any combination and subcombinations (including multiple dependent combinations and subcombinations), with one or more other features described herein. The various features described or illustrated above, including any components thereof, may be combined or integrated in other systems. Moreover, certain features may be omitted or not implemented. Examples of changes, substitutions, and alterations are ascertainable by one skilled in the art and could be made without departing from the scope of the information disclosed herein. All references cited herein are incorporated by reference in their entirety and made part of this application.

Claims (14)

What is claimed is:
1. A photoactivatable fiber, wherein the photoactivatable fiber comprises:
at least one thermoplastic polymer selected from one or more of acrylonitrile butadiene styrene (ABS), polyether sulfone (PES), polyetherether ketone (PEEK), polyphenylene oxide (PPO), polybutylene, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polymethyl methacrylate polyester, and poly(methyl methacrylate) (PMMA), and
at least one xanthene dye;
wherein the at least one xanthene dye is compounded and extruded with the at least one thermoplastic polymer;
wherein the at least one xanthene dye is present in the at least one thermoplastic polymer at a concentration of between about 10 g/L and about 100 g/L of the total volume of the at least one thermoplastic polymer; and
wherein the photoactivatable fiber is responsive to actinic light to emit fluorescent light having a power density of between about 0.005 mW/cm2 to about 8 mW/cm2.
2. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is uniformly dispersed throughout the photoactivatable fiber.
3. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is non-uniformly dispersed throughout the photoactivatable fiber.
4. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is layered on the surface of the photoactivatable fiber.
5. The photoactivatable fiber as defined in claim 4, wherein the photoactivatable fiber comprises at least one layer of the at least one xanthene dye on its surface.
6. The photoactivatable fiber as defined in claim 4, wherein the photoactivatable fiber comprises more than one layer of the at least one xanthene dye on its surface.
7. The photoactivatable fiber as defined in claim 1, wherein the at least one thermoplastic polymer is one or more of polybutylene terephthalate (PBT), and poly(methyl methacrylate) (PMMA).
8. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is selected from the group consisting of Eosin Y, Eosin B, Erythrosine, Fluorescein, Rose Bengal and any mixture thereof.
9. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is Eosin Y.
10. The photoactivatable fiber as defined in claim 1, wherein the at least one xanthene dye is responsive to actinic light to emit light having a wavelength of between about 400 nm and about 800 nm.
11. The photoactivatable fiber as defined in claim 1, the photoactivatable fiber having a linear mass density of between 400 Deniers and 480 Deniers.
12. The photoactivatable fiber as defined in claim 1, further comprising a lubricant.
13. A photoactivatable fabric comprising a plurality of photoactivatable fibers wherein the photoactivatable fibers comprise:
i) at least one thermoplastic polymer selected from one or more of acrylonitrile butadiene styrene (ABS), polyether sulfone (PES), polyetherether ketone (PEEK), polyphenylene oxide (PPO), polybutylene, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polymethyl methacrylate polyester, and poly(methyl methacrylate) (PMMA), and
ii) at least one xanthene dye, wherein the at least one xanthene dye is compounded and extruded into the photoactivatable fibers;
wherein the at least one xanthene dye is present in the at least one thermoplastic polymer at a concentration of between about 10 g/L and about 100 g/L of the total volume of the at least one thermoplastic polymer; and
wherein the photoactivatable fibers are responsive to actinic light to emit fluorescent light having a power density of between about 0.005 mW/cm2 to about 8 mW/cm2.
14. A method for effecting phototherapy on a subject, the method comprising:
applying a photoactivatable fiber onto the subject, wherein the photoactivatable fiber comprises at least one thermoplastic polymer selected from one or more of acrylonitrile butadiene styrene (ABS), polyether sulfone (PES), polyetherether ketone (PEEK), polyphenylene oxide (PPO), polybutylene, polyethylene terephthalate (PET), polybutylene terephthalate (PBT), polymethyl methacrylate polyester, and poly(methyl methacrylate) (PMMA), and at least one xanthene dye; wherein the at least one xanthene dye is compounded and extruded with the at least one thermoplastic polymer;
wherein the at least one xanthene dye is present in the at least one thermoplastic polymer at a concentration of between about 10 g/L and about 100 g/L of the total volume of the at least one thermoplastic polymer; and
illuminating the photoactivatable fiber; wherein illumination of the photoactivatable fiber causes the photoactivatable fiber to emit fluorescent light having a power density of between about 0.005 mW/cm2 to about 8 mW/cm2.
US15/523,283 2014-10-31 2015-10-30 Photoactivatable fibers and fabric media Active US11421349B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US15/523,283 US11421349B2 (en) 2014-10-31 2015-10-30 Photoactivatable fibers and fabric media

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462073795P 2014-10-31 2014-10-31
US15/523,283 US11421349B2 (en) 2014-10-31 2015-10-30 Photoactivatable fibers and fabric media
PCT/CA2015/051118 WO2016065488A1 (en) 2014-10-31 2015-10-30 Photoactivatable fibers and fabric media

Publications (2)

Publication Number Publication Date
US20170362744A1 US20170362744A1 (en) 2017-12-21
US11421349B2 true US11421349B2 (en) 2022-08-23

Family

ID=55856323

Family Applications (1)

Application Number Title Priority Date Filing Date
US15/523,283 Active US11421349B2 (en) 2014-10-31 2015-10-30 Photoactivatable fibers and fabric media

Country Status (14)

Country Link
US (1) US11421349B2 (en)
EP (1) EP3212826B1 (en)
JP (2) JP2018500468A (en)
KR (1) KR20170077153A (en)
CN (1) CN107075738B (en)
AR (1) AR102493A1 (en)
AU (1) AU2015337786B2 (en)
BR (1) BR112017008849B1 (en)
CA (1) CA2966010C (en)
ES (1) ES2856841T3 (en)
IL (1) IL252012A0 (en)
MX (1) MX380590B (en)
RU (1) RU2017117187A (en)
WO (1) WO2016065488A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11998759B2 (en) 2018-08-21 2024-06-04 Lumia Group, LLC Electrically passive low-level light therapy system and methods incorporating same

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130281913A1 (en) 2012-04-20 2013-10-24 Klox Technologies Inc. Biophotonic compositions and methods for providing biophotonic treatment
US11116841B2 (en) 2012-04-20 2021-09-14 Klox Technologies Inc. Biophotonic compositions, kits and methods
RU2016103321A (en) 2013-07-03 2017-08-08 Клокс Текнолоджиз Инк. COMPOSITIONS AND METHODS FOR TREATING NON-HEALING RAS
KR20160140716A (en) 2014-04-01 2016-12-07 클록스 테크놀로지스 인크. Tissue filler compositions and methods of use
AU2015337786B2 (en) 2014-10-31 2020-03-26 Klox Technologies Inc. Photoactivatable fibers and fabric media
US20200222536A1 (en) * 2016-05-23 2020-07-16 Orphaderm Limited Biophotonic compositions comprising a fungal-derived chromophore
WO2018201257A1 (en) * 2017-05-04 2018-11-08 Klox Technologies Inc. Absorbent biophotonic devices and systems for wound healing
KR101957439B1 (en) * 2018-02-20 2019-03-12 김태건 Material comprising 2,5-bis(5-tert-butyl-2-benzoxazolyl)thiophene for multifunctional fiber, and multifunctional fiber and master batch comprising the same
WO2019232628A1 (en) * 2018-06-05 2019-12-12 Klox Technologies Inc. Absorbent biophotonic fiber system
CN109295747A (en) * 2018-08-09 2019-02-01 青岛大学 A fluorescent knitted fabric
WO2021003568A1 (en) * 2019-07-08 2021-01-14 Klox Technologies Inc. Inert polymer-coated biophotonic systems
JP7353117B2 (en) * 2019-10-03 2023-09-29 三菱瓦斯化学株式会社 Films, security cards, passports, fibrous molded objects, and methods for determining authenticity
CN111021104A (en) * 2019-12-12 2020-04-17 苏州麻朵纺织科技有限公司 Natural dyeing auxiliary for dyeing medium and light color series and dyeing method thereof

Citations (209)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2877221A (en) 1954-03-17 1959-03-10 Pfizer & Co C 11, 14-peroxides of substituted ergostadiene compounds
US3107968A (en) * 1961-02-17 1963-10-22 Du Pont Dyeing of acid-modified acrylic and polyester fibers
US3293127A (en) 1964-07-22 1966-12-20 Gold Crest Chemical Corp Inc Arterial embalming fluid and method for embalming therewith
US3309274A (en) 1962-07-23 1967-03-14 Brilliant Herbert Use of fluorescent dyes in dental diagnostic methods
US3336923A (en) * 1963-11-29 1967-08-22 Rodofrand Corp Sterile absorbent pads
US3372125A (en) 1965-11-15 1968-03-05 Peter Strong & Company Inc Denture cleanser
US3595798A (en) 1967-12-18 1971-07-27 Lever Brothers Ltd Cleansing compositions
US3597362A (en) 1965-09-08 1971-08-03 American Cyanamid Co Generation of light by the reaction of esters of oxalic-type acids
US3652420A (en) 1964-07-24 1972-03-28 Peter Strong & Co Inc Cleanser compositons for artificial dentures and methods of preparing the same
US3671450A (en) 1969-09-22 1972-06-20 American Cyanamid Co Chemiluminescent compositions
US3728446A (en) 1971-01-11 1973-04-17 Colgate Palmolive Co Speckled dentifrice gel
US3795530A (en) * 1968-04-26 1974-03-05 Xerox Corp Electrostatic latent image development
WO1981000513A1 (en) 1979-08-20 1981-03-05 J Thorel New compositions for detecting dental plaque
DE2935450A1 (en) 1979-09-01 1981-03-19 Hermann Dr.Med.Dent. 4044 Kaarst Gertenbach Tooth cleansing compsn. contg. dye - pref. encapsulated in gelatin to indicate presence of tooth deposit e.g. plaque
US4320140A (en) 1980-10-09 1982-03-16 Sterling Drug Inc. Synergistic insecticidal compositions
JPS60199942A (en) 1984-03-24 1985-10-09 チッソ株式会社 Fiber product having fluorescence
US4574097A (en) 1984-08-10 1986-03-04 Isopedix Corporation Reinforced thixotropic gel composition
JPH01111075A (en) 1987-10-19 1989-04-27 Kanebo Ltd Light accumulating fiber
JPH01279838A (en) 1988-04-30 1989-11-10 Kiyuukiyuu Yakuhin Kogyo Kk Lysozyme chloride-containing plaster for gingivitis and pyorrhea
US4891211A (en) 1988-06-29 1990-01-02 Church & Dwight Co., Inc. Stable hydrogen peroxide-releasing dentifice
US4923726A (en) 1988-12-05 1990-05-08 Somar Corporation Lightsafe masking film
EP0380157A1 (en) 1989-01-24 1990-08-01 Yosef David Weisberg Wound healing powder
WO1990009779A1 (en) 1989-02-28 1990-09-07 Benhuri Marc N Method and composition for treatment of periodontal disease
US4992256A (en) 1989-09-27 1991-02-12 Colgate-Palmolive Company Plaque disclosing compositions
WO1991002530A1 (en) 1989-08-25 1991-03-07 Sunstar Kabushiki Kaisha Accelerator for periodontal tissue regeneration
JPH04219756A (en) 1990-03-09 1992-08-10 Hoechst Ag Optical polymerizing mixture and recording material prepared therefrom
JPH0649771A (en) * 1992-05-18 1994-02-22 Minnesota Mining & Mfg Co <3M> Non-woven fabric with reverse reflection of fluorescence
US5292362A (en) 1990-07-27 1994-03-08 The Trustees Of Columbia University In The City Of New York Tissue bonding and sealing composition and method of using the same
JPH06128807A (en) 1992-10-16 1994-05-10 Mitsubishi Rayon Co Ltd Fluorescent chromogenic fiber and method for producing
EP0704539A2 (en) 1994-08-29 1996-04-03 JOHNSON &amp; JOHNSON CLINICAL DIAGNOSTICS, INC. Chemiluminescent reagent and assay using a substituted acetanilide for light generation
US5516227A (en) 1994-07-07 1996-05-14 Iit Research Institute Spherodized fluorescent beads for improved roadway pavement marker visibility
JPH08127937A (en) 1994-11-01 1996-05-21 Nemoto Tokushu Kagaku Kk Textile products with phosphorescent fluorescence
CA2166527A1 (en) 1995-01-05 1996-07-06 William Guy Love Topical pharmaceutical compositions
JPH092925A (en) 1995-06-16 1997-01-07 Shiseido Co Ltd Two agent-mixing type cosmetic
US5611793A (en) 1992-04-30 1997-03-18 Institute Of Dental Surgery Laser treatment
WO1997021420A1 (en) 1995-12-12 1997-06-19 Britesmile, Inc. Method for whitening teeth
US5658148A (en) 1995-04-26 1997-08-19 Ceramoptec Industries, Inc. Dental laser brushing or cleaning device
US5677028A (en) * 1996-04-09 1997-10-14 Wearever Health Care Products, Llc Absorbent material
WO1998010738A1 (en) 1996-09-16 1998-03-19 The Procter & Gamble Company Antimicrobial oral care compositions
WO1998011827A1 (en) 1996-09-19 1998-03-26 The General Hospital Corporation Modulation of wound healing by photodynamic therapy
US5749968A (en) 1993-03-01 1998-05-12 Focal, Inc. Device for priming for improved adherence of gels to substrates
WO1998023219A1 (en) 1996-11-27 1998-06-04 Sibner Jeffrey A Dental bleaching composition and method
CA2222027A1 (en) 1996-12-05 1998-06-05 Centre International De Recherches Dermatologiques Galderma Use of a chromophore in a composition to be applied to the skin before a laser treatment
JPH10182390A (en) 1996-12-25 1998-07-07 Lion Corp Oral composition
WO1998030169A1 (en) 1997-01-10 1998-07-16 Ultradent Products, Inc. Stable light or heat activated dental bleaching compositions
WO1998033761A1 (en) 1997-01-30 1998-08-06 Ciba Specialty Chemicals Holding Inc. Non-volatile phenylglyoxalic esters
US5844016A (en) 1995-03-23 1998-12-01 Focal, Inc. Redox and photoinitiator priming for improved adherence of gels to substrates
JPH10330235A (en) 1997-06-02 1998-12-15 Lion Corp Denture cleaner
US5858332A (en) 1997-01-10 1999-01-12 Ultradent Products, Inc. Dental bleaching compositions with high concentrations of hydrogen peroxide
US5885557A (en) 1996-02-08 1999-03-23 Estee Lauder Inc. Compositions useful in the phototherapeutic treatment of proliferative skin disorders
US5914076A (en) * 1997-10-10 1999-06-22 The Glo-Tech Corporation Process for producing longer-lasting, high luminescence, phosphorescent textile fibers
US5922331A (en) 1997-03-26 1999-07-13 Chanel, Inc. Skin cream composition
WO1999039238A1 (en) 1998-01-28 1999-08-05 Keratoform, Inc. Methods and apparatus for accelerated orthokeratology
WO1999040870A1 (en) 1998-02-13 1999-08-19 Britesmile, Inc. Light-activated tooth whitening composition and method of using same
WO1999049823A1 (en) 1998-03-30 1999-10-07 Fibermark, Inc. Light-activated antimicrobial polymeric materials
US5977199A (en) 1998-02-17 1999-11-02 The Kerr Corporation Composition, delivery system therefor, and method for making temporary crowns and bridges
WO1999063900A1 (en) 1998-06-12 1999-12-16 Photogen, Inc. Improved methods and apparatus for multi-photon photo-activation of therapeutic agents
US6030222A (en) 1998-12-01 2000-02-29 Tarver; Jeanna G. Dye compositions and methods for whitening teeth using same
US6036493A (en) 1998-07-23 2000-03-14 Ad Dent Inc. Dental bleaching system and method
US6056548A (en) 1995-04-26 2000-05-02 Ceramoptec Industries, Inc. Hygienic dental laser photo treatment method
US6084005A (en) 1997-02-24 2000-07-04 Kuraray Co., Ltd. Antimicrobial caries-detecting composition
CA2360202A1 (en) 1999-01-04 2000-07-13 Richard Rox Anderson Energy activatable material for the treatment of sebaceous gland disorders
US6121341A (en) 1995-03-23 2000-09-19 Board Of Regents, The University Of Texas System Redox and photoinitiator systems for priming and improved adherence of gels to substrates
US6149895A (en) 1998-02-17 2000-11-21 Kreativ, Inc Dental bleaching compositions, kits & methods
US6162055A (en) 1998-02-13 2000-12-19 Britesmile, Inc. Light activated tooth whitening composition and method of using same
WO2001000190A2 (en) 1999-06-29 2001-01-04 Fidia Advanced Biopolymers, S.R.L. Hyaluronic acid derivatives for the prevention and treatment of cutaneous scars
WO2001012181A1 (en) 1999-08-13 2001-02-22 Photogen, Inc. Improved topical medicaments and methods for photodynamic treatment of disease
US6217794B1 (en) * 1998-06-01 2001-04-17 Isotag Technology, Inc. Fiber coating composition having an invisible marker and process for making same
US6267976B1 (en) 2000-04-14 2001-07-31 Gojo Industries, Inc. Skin cleanser with photosensitive dye
US20010022970A1 (en) 1996-10-30 2001-09-20 Photogen, Inc. Intracorporeal medicaments for photodynamic treatment of disease
US20010045677A1 (en) * 1999-09-24 2001-11-29 Kyeng-Jung Kang Phosphorescent fiber and method of manufacturing the same
WO2002011539A1 (en) 2000-08-08 2002-02-14 Cytopharm, Inc. Methods and compositions for treating skin ulcers by topical photodynamic therapy
WO2002022097A1 (en) 2000-09-14 2002-03-21 High Tech Laser Method and composition for dental bleaching
US6365134B1 (en) 1999-07-07 2002-04-02 Scientific Pharmaceuticals, Inc. Process and composition for high efficacy teeth whitening
US6387353B1 (en) 1997-01-10 2002-05-14 Ultradent Products, Inc. Light or heat activated dental bleaching compositions
US6420455B1 (en) 1999-06-18 2002-07-16 3M Innovative Properties Company Antimicrobial composition containing photosensitizers articles, and methods of use
JP2002226349A (en) 2001-01-23 2002-08-14 Addent Inc Dental bleaching composition, activating agent system, and method for applying and activating the dental bleaching composition
JP2002233612A (en) 2001-02-07 2002-08-20 Daito Giken:Kk Gable table
EP1235543A1 (en) 1999-12-08 2002-09-04 The Procter & Gamble Company Tartar control denture adhesive compositions
EP1235544A1 (en) 1999-12-08 2002-09-04 The Procter & Gamble Company Tartar control denture adhesive compositions
JP2002293747A (en) 2001-03-29 2002-10-09 Jinen:Kk Skin preparation for external use
US20020157165A1 (en) * 1997-09-11 2002-10-31 Kroll Mark W. Light selective sports garments
WO2003000215A1 (en) 2001-06-21 2003-01-03 Herbariorum Medicaminum Officina Alta Badiae S.N.C. Tooth-paste composition having anti-plaque properties
WO2003017824A2 (en) 1998-11-30 2003-03-06 Light Bioscience, Inc. Method and apparatus for acne treatment
US6541460B2 (en) 1996-08-07 2003-04-01 George D. Petito Method for use of hyaluronic acid in wound management
US20030085384A1 (en) * 1998-10-13 2003-05-08 Peter Burnell-Jones Heat curable thermosetting luminescent resins
WO2003061696A2 (en) 2002-01-23 2003-07-31 Light Sciences Corporation Systems and methods for photodynamic therapy
US20030157323A1 (en) * 2001-05-14 2003-08-21 Mikhail Khavkine Hybrid yarns which include oil seed flax plant bast fiber and other fibers and fabrics made with such yarns
WO2003086215A1 (en) 2002-04-11 2003-10-23 Light Bioscience, Inc. Low intensity light therapy for the manipulation of fibroblast-derived mammalian cells and collagen
US20030198605A1 (en) 1998-02-13 2003-10-23 Montgomery R. Eric Light-activated tooth whitening composition and method of using same
JP2003339875A (en) 2003-06-16 2003-12-02 Hirokatsu Kimura Tatoo eliminating device
WO2003099247A1 (en) 2002-05-23 2003-12-04 The Procter & Gamble Company Tooth whitening products
WO2004028498A1 (en) 2002-09-24 2004-04-08 The Boots Company Plc Dental compositions and methods
US20040136971A1 (en) 2002-10-11 2004-07-15 David Scharp Implantation of encapsulated biological materials for treating diseases
US20040147508A1 (en) * 2001-05-30 2004-07-29 Photopharmica Limited Biologically active methylene blue derivatives
WO2004081222A2 (en) 2003-03-14 2004-09-23 Sol-Gel Technologies Ltd. Agent-encapsulating micro- and nanoparticles, methods for preparation of same and products containing same
US20040191330A1 (en) 2003-03-31 2004-09-30 Keefe Candace R. Daily skin care regimen
WO2004104277A1 (en) 2003-05-22 2004-12-02 Landqart Photoluminescent fibre, security paper and other security articles
US20040262569A1 (en) 2003-06-24 2004-12-30 Lg.Philips Lcd Co., Ltd. Etchant for etching double-layered copper structure and method of forming array substrate having double-layered copper structures
US6849330B1 (en) * 2003-08-30 2005-02-01 Milliken & Company Thermoplastic fibers exhibiting durable high color strength characteristics
US20050026298A1 (en) 2003-08-01 2005-02-03 Tim Bickett Dye solutions for use in methods to detect the prior evaporation of anhydrous ammonia and the production of illicit drugs
WO2005009604A1 (en) 2003-07-31 2005-02-03 Sol-Gel Technologies Ltd. Microcapsules loaded with active ingredients and a method for their preparation
US20050042712A1 (en) 2003-08-22 2005-02-24 Advanced Medical Optics, Inc. Methods, compositions and instruments to predict antimicrobial or preservative activity
US20050042428A1 (en) * 2003-08-22 2005-02-24 Dean David M. Methods for identity verification using transparent luminescent polymers
US20050059731A1 (en) 2003-09-16 2005-03-17 Ceramoptec Industries, Inc. Erythrosin-based antimicrobial photodynamic therapy compound and its use
US20050098766A1 (en) 2002-09-19 2005-05-12 Watson David L.Jr. Chemiluminescent processes and systems
US20050123588A1 (en) 2003-06-16 2005-06-09 Zhu Yong H. Deployable multifunctional hemostatic agent
WO2005051305A2 (en) 2003-11-19 2005-06-09 Barnes-Jewish Hospital Enhanced drug delivery
US6905672B2 (en) 1999-12-08 2005-06-14 The Procter & Gamble Company Compositions and methods to inhibit tartar and microbes using denture adhesive compositions with colorants
US20050244455A1 (en) * 2004-04-20 2005-11-03 Greenawalt Keith E Surgical prosthesis
CA2551613A1 (en) 2004-05-21 2005-12-01 Tottori University A composition comprising n-acetyl-d-glucosamine for treatment of wound
CA2580381A1 (en) 2004-06-18 2006-01-26 The Ohio State University Research Foundation Methods and compositions for wound healing
WO2006014597A1 (en) 2004-07-08 2006-02-09 3M Innovative Properties Company Dental methods, compositions, and kits including acid-sensitive dyes
WO2006032847A1 (en) 2004-09-20 2006-03-30 Photopharmica Limited Wound healing
WO2006047868A1 (en) 2004-11-02 2006-05-11 John Kennedy Method of treating microorganisms in the oral cavity via photodynamic therapy employing a non-coherent light source
US7066941B2 (en) 2001-07-09 2006-06-27 Perricone Nicholas V Apparatus for skin treatment
WO2006072243A1 (en) 2005-01-03 2006-07-13 Novozymes Biopolymer A/S Hyaluronic acid fraction with moisturizing and anti-wrinkle properties
US7081128B2 (en) 2002-03-04 2006-07-25 Hart Barry M Phototherapy device and method of use
US20060199242A1 (en) 2005-03-01 2006-09-07 Ching-Ying Cheung Chemical probe compounds that become fluorescent upon reduction, and methods for their use
US20060217690A1 (en) 2005-03-22 2006-09-28 Bastin Norman J Method for treating various dermatological and muscular conditions using electromagnetic radiation
WO2006118835A2 (en) 2005-04-29 2006-11-09 Johnson & Johnson Consumers Companies, Inc. Topical composition fluorescence detection
WO2006125650A1 (en) 2005-05-25 2006-11-30 3M Espe Ag Dental composition for detection of carious tissue, detection method
WO2006135344A1 (en) 2005-06-13 2006-12-21 National University Of Singapore A photosensitising composition and uses thereof
US20070016173A1 (en) * 2005-07-14 2007-01-18 Michael Kreindel Protective material, clothing item and method of protection
US20070021807A1 (en) 2005-07-20 2007-01-25 Eastman Kodak Company Device for optically stimulating collagen formation in tissue
KR20070017292A (en) 2003-09-16 2007-02-09 세람옵텍 인더스트리스, 인크. Erythrosine-Based Antimicrobial Photodynamic Therapeutic Compounds and Uses thereof
WO2007025244A2 (en) 2005-08-25 2007-03-01 Houle Philip R Treatment systems for delivery of sensitizer solutions
US20070092469A1 (en) 2005-10-26 2007-04-26 Eric Jacobs Topically applied Glucosamine Sulfate and all its related, precursor, and derivative compounds significantly increases the skin's natural produciton of hyaluronic acid for the rejuvenation of healthier younger-looking skin; while PhosphatidylCholine is required to replace its deficiency caused by topical Dimethylaminoethanol (DMAE)
EP1779891A1 (en) 2005-10-28 2007-05-02 Abdula Kurkayev Method of activating a photosensitizer
US20070128132A1 (en) 2005-11-09 2007-06-07 Remigio Piergallini Teeth whitening composition and methods
US20070142762A1 (en) * 2005-12-16 2007-06-21 Eastman Kodak Company Wound dressing
US20070149722A1 (en) * 2004-08-05 2007-06-28 General Electric Company Flame retardant thermoplastic polycarbonate compositions, method of manufacture, and method of use thereof
US20070166369A1 (en) 2006-01-18 2007-07-19 Ceramoptec Industries, Inc. Photodynamic cosmetic procedure and healing method
WO2007087259A2 (en) 2006-01-23 2007-08-02 The Procter & Gamble Company Enzyme and photobleach containing compositions
US20070244195A1 (en) 2004-05-18 2007-10-18 Burkhart Craig N Treatment methods with peroxides and tertiary amines
WO2007127172A2 (en) 2006-04-27 2007-11-08 The Trustees Of Columbia University In The City Of New York Layered bio-adhesive compositions and uses thereof
US20070288071A1 (en) * 2006-06-07 2007-12-13 Rogers Gary S Continuous low irradiance photodynamic therapy system and method
US20070290172A1 (en) * 2006-06-19 2007-12-20 General Electric Company Infrared transmissive thermoplastic composition, and articles formed therefrom
US7314470B2 (en) 2000-11-04 2008-01-01 Wolfgang Malodobry Scar-free removal of tattoos
WO2008011707A1 (en) 2006-07-24 2008-01-31 Quest Pharmatech Inc. Method and device for photodynamic therapy
WO2008013962A2 (en) 2006-07-28 2008-01-31 Ceramoptec Industries, Inc. Method and mixture for in-vivo photochemical cross-linking of collagen
US20080058689A1 (en) 2002-06-12 2008-03-06 University Of Florida Research Foundation, Inc. Phototherapy bandage
US20080060148A1 (en) * 2005-03-09 2008-03-13 Pinyayev Aleksey M Sensor responsive electric toothbrushes and methods of use
US7354448B2 (en) 2001-11-29 2008-04-08 Palomar Medical Technologies, Inc. Dental phototherapy methods and compositions
WO2008052081A2 (en) 2006-10-24 2008-05-02 California Institute Of Technology Photochemical therapy to affect mechanical and/or chemical properties of body tissue
US20080108681A1 (en) 2006-10-27 2008-05-08 Access Business Group International Llc Use of allantoin as a pro-collagen synthesis agent in cosmetic compositions
US20080113037A1 (en) 2006-11-10 2008-05-15 Green Barbara A Topical Compositions Comprising Polyhydroxy Acids and/or Lactones for Improved Cutaneous Effects of Oxidative Therapeutic Drugs
US20080118578A1 (en) 1997-12-11 2008-05-22 Dees H Craig Topical Medicaments and Methods for Photodynamic Treatment of Disease
US20080138289A1 (en) 2006-12-08 2008-06-12 Evident Technologies, Inc. Systems and methods for detecting infrared emitting composites and medical applications therefor
US20080206159A1 (en) 2003-08-04 2008-08-28 Foamix Ltd. Compositions with modulating agents
US20080262154A1 (en) * 2005-12-22 2008-10-23 Basf Se Aqueous Dispersions of Polymers which Comprise a Fluorescent Dye, Process for Their Production and Their Use for Marking Materials
US20080305101A1 (en) 2007-01-03 2008-12-11 Erkki Ruoslahti Methods and Compositions Related to Clot Binding Compounds
US20090036593A1 (en) * 2007-07-31 2009-02-05 Sabic Innovative Plastics Ip Bv Polycarbonate compositions with improved molding capability
US20090041984A1 (en) * 2007-08-10 2009-02-12 Nano Terra Inc. Structured Smudge-Resistant Coatings and Methods of Making and Using the Same
WO2009089346A2 (en) 2008-01-08 2009-07-16 Quick-Med Technologies, Inc. Disinfectant alcohol-soluble quaternary ammonium polymers
CA2706808A1 (en) 2007-11-27 2009-08-06 Michele Eymard Du Vernet Composition for photodynamic skin treatment
US20090246251A1 (en) * 2008-03-27 2009-10-01 Affinergy Coating compositions having improved performance
US7611831B2 (en) * 1998-01-06 2009-11-03 Cerus Corporation Adsorbing pathogen-inactivating compounds with porous particles immobilized in a matrix
US20100040809A1 (en) * 2006-12-27 2010-02-18 Mueller Daniel Multifilament, monofilament, non-woven or tape
US20100063467A1 (en) * 2006-07-13 2010-03-11 Deborah Addison Hydrogel Wound Dressings Exhibiting Reduced Fiber Losses in Use
CA2738035A1 (en) 2008-09-29 2010-04-01 Mallinckrodt Inc. Dithienopyrrole dyes for imaging and therapy
WO2010051641A1 (en) 2008-11-07 2010-05-14 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US20100125963A1 (en) * 2008-11-21 2010-05-27 E. I. Du Pont De Nemours And Company Monofilament comprising hydrophilic agent
WO2010070292A1 (en) 2008-12-20 2010-06-24 Convatec Technologies Inc A composition for use on skin and wound
US20100159769A1 (en) * 2008-12-19 2010-06-24 Macdonald John G Plasticizer for thermoplastic materials
US20100227799A1 (en) 2009-03-09 2010-09-09 Medtronic Vascular, Inc. Simultaneous photodynamic therapy and photo induced polymerization
GB2469219A (en) * 2008-04-10 2010-10-06 Kythera Biopharmaceuticals Inc Dermal filler composition
US20100266989A1 (en) 2006-11-09 2010-10-21 Klox Technologies Inc. Teeth whitening compositions and methods
WO2010151563A1 (en) 2009-06-25 2010-12-29 3M Innovative Properties Company Light-activated antimicrobial article and method of use
WO2011006263A1 (en) 2009-07-17 2011-01-20 Klox Technologies Inc. Antibacterial oral composition
JP2011063889A (en) 2009-09-15 2011-03-31 Fujifilm Corp Cross-spray electric field spinning
WO2011058448A2 (en) 2009-10-27 2011-05-19 Klox Technologies Inc. Device for personal use in phototherapy
US20110143621A1 (en) * 2009-12-10 2011-06-16 Macdonald John Gavin Plasticizer for thermoplastic polymer materials
US20110171310A1 (en) 2010-01-13 2011-07-14 Allergan Industrie, Sas Hydrogel compositions comprising vasoconstricting and anti-hemorrhagic agents for dermatological use
CN102133208A (en) 2011-03-17 2011-07-27 北京化工大学 Photosensitive microcapsule used for photodynamic therapy and preparation method thereof
US20110245748A1 (en) 2008-10-01 2011-10-06 Action Bandage, Llc Wound care device
US20110313407A1 (en) * 2010-06-18 2011-12-22 Rafailov Edik U Quantum-dot laser diode
CA2809405A1 (en) 2010-07-21 2012-01-26 Republic Polytechnic Compounds for photodynamic therapy
US20120080613A1 (en) * 2010-09-30 2012-04-05 Performance Indicator, Llc. Photolytically and Environmentally Stable Multilayer Structure for High Efficiency Electromagnetic Energy Conversion and Sustained Secondary Emission
US20120116391A1 (en) * 2010-11-05 2012-05-10 Houser Kevin L Surgical instrument with sensor and powered control
US8182473B2 (en) 1999-01-08 2012-05-22 Palomar Medical Technologies Cooling system for a photocosmetic device
WO2012072980A1 (en) 2010-11-30 2012-06-07 Convatec Technologies Inc A composition for detecting biofilms on viable tissues
JP2012512932A (en) 2008-12-19 2012-06-07 キンバリー クラーク ワールドワイド インコーポレイテッド Plasticizers for thermoplastic polymer materials
US20120157576A1 (en) * 2010-12-16 2012-06-21 Ticona Llc Polyoxymethylene Fibers in Concrete
US20120283622A1 (en) * 2009-11-10 2012-11-08 Nath Guenther Dermatological treatment device
US20130060183A1 (en) * 2011-09-02 2013-03-07 John Cuevas Ramirez Attachable grip enhancers and uses and methods of said enhancers
US20130115843A1 (en) * 2010-04-23 2013-05-09 Pegas Nonwovens S.R.O. Method of producing a nonwoven textile comprising a barrier and an antistatic treatment
WO2013113349A1 (en) 2012-01-30 2013-08-08 Merck Patent Gmbh Nanocrystals on fibers
CA2868893A1 (en) 2012-04-20 2013-10-24 Klox Technologies Inc. Biophotonic compositions, kits and methods
WO2014040177A1 (en) 2012-09-14 2014-03-20 Klox Technologies Inc. Cosmetic biophotonic compositions
WO2014040176A1 (en) 2012-09-14 2014-03-20 Klox Technologies Inc. Chromophore combinations for biophotonic uses
US20140082859A1 (en) * 2011-12-21 2014-03-27 Shaw Industries Group, Inc. System and method for space-dyeing yarn
US20140105832A1 (en) * 2012-09-14 2014-04-17 Valeant Pharmaceuticals International, Inc. Compositions and methods for teeth whitening
US20140128943A1 (en) * 2012-11-07 2014-05-08 Rogers Sciences, Inc. Implantable clipt illumination system
US20140161850A1 (en) 2012-12-11 2014-06-12 Elc Management Llc Cosmetic Compositions With Near Infra-Red (NIR) Light - Emitting Material And Methods Therefor
US20140276354A1 (en) 2013-03-14 2014-09-18 Klox Technologies Inc. Biophotonic materials and uses thereof
US20140260437A1 (en) * 2013-03-13 2014-09-18 Robert H. Fleming, Jr. Skin-Contacting Tubular Fabric Underlay For Use Beneath A Therapeutic or Prosthetic Device
US20140303547A1 (en) 2013-03-01 2014-10-09 Klox Technologies Inc. Phototherapeutic device, method and use
US20140306869A1 (en) * 2011-09-21 2014-10-16 Sharp Kabushiki Kaisha Transition metal complex having alkoxy group, organic light-emitting device using same, color conversion light-emitting device using same, light conversion light-emitting device using same, organic laser diode light-emitting device using same, dye laser using same, display system using same, lighting system using same, and electronic equipment using same
US20140308867A1 (en) * 2011-04-19 2014-10-16 Ar Metallizing N.V. Antimicrobial nonwoven fabric
US20140309717A1 (en) * 2008-01-16 2014-10-16 Morgan Lars Ake Gustavsson Fluorescent handpiece
WO2015000058A1 (en) 2013-07-03 2015-01-08 Klox Technologies Inc. Biophotonic compositions comprising a chromophore and a gelling agent for treating wounds
US20150119788A1 (en) 2012-04-20 2015-04-30 Klox Technologies Inc. Biophotonic compositions, kits and methods
WO2015184551A1 (en) 2014-06-04 2015-12-10 Klox Technologies Inc. Biophotonic hydrogels
WO2016065488A1 (en) 2014-10-31 2016-05-06 Klox Technologies Inc. Photoactivatable fibers and fabric media
US20160205925A1 (en) * 2015-01-15 2016-07-21 Ariel-University Research And Development Company Ltd. Antimicrobial compositions made of a thermoplastic polymer and a photosensitizer
US20170209348A1 (en) * 2014-06-24 2017-07-27 Klox Technologies Inc. Biophotonic compositions comprising halogen and uses thereof
WO2017201615A1 (en) 2016-05-23 2017-11-30 Orphaderm Limited Biophotonic compositions comprising a fungal-derived chromophore
US20200063299A1 (en) * 2016-11-01 2020-02-27 Teijin Limited Fabric, method for manufacturing same, and fiber product

Patent Citations (269)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2877221A (en) 1954-03-17 1959-03-10 Pfizer & Co C 11, 14-peroxides of substituted ergostadiene compounds
US3107968A (en) * 1961-02-17 1963-10-22 Du Pont Dyeing of acid-modified acrylic and polyester fibers
US3309274A (en) 1962-07-23 1967-03-14 Brilliant Herbert Use of fluorescent dyes in dental diagnostic methods
US3336923A (en) * 1963-11-29 1967-08-22 Rodofrand Corp Sterile absorbent pads
US3293127A (en) 1964-07-22 1966-12-20 Gold Crest Chemical Corp Inc Arterial embalming fluid and method for embalming therewith
US3652420A (en) 1964-07-24 1972-03-28 Peter Strong & Co Inc Cleanser compositons for artificial dentures and methods of preparing the same
US3597362A (en) 1965-09-08 1971-08-03 American Cyanamid Co Generation of light by the reaction of esters of oxalic-type acids
US3372125A (en) 1965-11-15 1968-03-05 Peter Strong & Company Inc Denture cleanser
US3595798A (en) 1967-12-18 1971-07-27 Lever Brothers Ltd Cleansing compositions
US3795530A (en) * 1968-04-26 1974-03-05 Xerox Corp Electrostatic latent image development
US3671450A (en) 1969-09-22 1972-06-20 American Cyanamid Co Chemiluminescent compositions
US3728446A (en) 1971-01-11 1973-04-17 Colgate Palmolive Co Speckled dentifrice gel
WO1981000513A1 (en) 1979-08-20 1981-03-05 J Thorel New compositions for detecting dental plaque
DE2935450A1 (en) 1979-09-01 1981-03-19 Hermann Dr.Med.Dent. 4044 Kaarst Gertenbach Tooth cleansing compsn. contg. dye - pref. encapsulated in gelatin to indicate presence of tooth deposit e.g. plaque
US4320140A (en) 1980-10-09 1982-03-16 Sterling Drug Inc. Synergistic insecticidal compositions
JPS60199942A (en) 1984-03-24 1985-10-09 チッソ株式会社 Fiber product having fluorescence
US4574097A (en) 1984-08-10 1986-03-04 Isopedix Corporation Reinforced thixotropic gel composition
JPH01111075A (en) 1987-10-19 1989-04-27 Kanebo Ltd Light accumulating fiber
JPH01279838A (en) 1988-04-30 1989-11-10 Kiyuukiyuu Yakuhin Kogyo Kk Lysozyme chloride-containing plaster for gingivitis and pyorrhea
US4891211A (en) 1988-06-29 1990-01-02 Church & Dwight Co., Inc. Stable hydrogen peroxide-releasing dentifice
US4923726A (en) 1988-12-05 1990-05-08 Somar Corporation Lightsafe masking film
EP0380157A1 (en) 1989-01-24 1990-08-01 Yosef David Weisberg Wound healing powder
WO1990009779A1 (en) 1989-02-28 1990-09-07 Benhuri Marc N Method and composition for treatment of periodontal disease
WO1991002530A1 (en) 1989-08-25 1991-03-07 Sunstar Kabushiki Kaisha Accelerator for periodontal tissue regeneration
US4992256A (en) 1989-09-27 1991-02-12 Colgate-Palmolive Company Plaque disclosing compositions
JPH03169805A (en) 1989-09-27 1991-07-23 Colgate Palmolive Co Composition for detecting tooth grime
JPH04219756A (en) 1990-03-09 1992-08-10 Hoechst Ag Optical polymerizing mixture and recording material prepared therefrom
US5292362A (en) 1990-07-27 1994-03-08 The Trustees Of Columbia University In The City Of New York Tissue bonding and sealing composition and method of using the same
US5611793A (en) 1992-04-30 1997-03-18 Institute Of Dental Surgery Laser treatment
US5478628A (en) * 1992-05-18 1995-12-26 Minnesota Mining And Manufacturing Company Non-woven fluorescent retrorefletive fabric
JPH0649771A (en) * 1992-05-18 1994-02-22 Minnesota Mining & Mfg Co <3M> Non-woven fabric with reverse reflection of fluorescence
JPH06128807A (en) 1992-10-16 1994-05-10 Mitsubishi Rayon Co Ltd Fluorescent chromogenic fiber and method for producing
US5749968A (en) 1993-03-01 1998-05-12 Focal, Inc. Device for priming for improved adherence of gels to substrates
US5516227A (en) 1994-07-07 1996-05-14 Iit Research Institute Spherodized fluorescent beads for improved roadway pavement marker visibility
EP0704539A2 (en) 1994-08-29 1996-04-03 JOHNSON &amp; JOHNSON CLINICAL DIAGNOSTICS, INC. Chemiluminescent reagent and assay using a substituted acetanilide for light generation
JPH08127937A (en) 1994-11-01 1996-05-21 Nemoto Tokushu Kagaku Kk Textile products with phosphorescent fluorescence
US5723148A (en) 1995-01-05 1998-03-03 Novartis Corp. Topical pharmaceutical compositions
CA2166527A1 (en) 1995-01-05 1996-07-06 William Guy Love Topical pharmaceutical compositions
US6121341A (en) 1995-03-23 2000-09-19 Board Of Regents, The University Of Texas System Redox and photoinitiator systems for priming and improved adherence of gels to substrates
US5844016A (en) 1995-03-23 1998-12-01 Focal, Inc. Redox and photoinitiator priming for improved adherence of gels to substrates
US6056548A (en) 1995-04-26 2000-05-02 Ceramoptec Industries, Inc. Hygienic dental laser photo treatment method
US5658148A (en) 1995-04-26 1997-08-19 Ceramoptec Industries, Inc. Dental laser brushing or cleaning device
JPH092925A (en) 1995-06-16 1997-01-07 Shiseido Co Ltd Two agent-mixing type cosmetic
WO1997021420A1 (en) 1995-12-12 1997-06-19 Britesmile, Inc. Method for whitening teeth
US6254388B1 (en) 1995-12-12 2001-07-03 Britesmile, Inc. Method for whitening teeth
US5885557A (en) 1996-02-08 1999-03-23 Estee Lauder Inc. Compositions useful in the phototherapeutic treatment of proliferative skin disorders
US5677028A (en) * 1996-04-09 1997-10-14 Wearever Health Care Products, Llc Absorbent material
US6541460B2 (en) 1996-08-07 2003-04-01 George D. Petito Method for use of hyaluronic acid in wound management
WO1998010738A1 (en) 1996-09-16 1998-03-19 The Procter & Gamble Company Antimicrobial oral care compositions
WO1998011827A1 (en) 1996-09-19 1998-03-26 The General Hospital Corporation Modulation of wound healing by photodynamic therapy
US6107466A (en) 1996-09-19 2000-08-22 The General Hospital Corporation Acceleration of wound healing by photodynamic therapy
US20010022970A1 (en) 1996-10-30 2001-09-20 Photogen, Inc. Intracorporeal medicaments for photodynamic treatment of disease
WO1998023219A1 (en) 1996-11-27 1998-06-04 Sibner Jeffrey A Dental bleaching composition and method
CA2222027A1 (en) 1996-12-05 1998-06-05 Centre International De Recherches Dermatologiques Galderma Use of a chromophore in a composition to be applied to the skin before a laser treatment
JPH10182390A (en) 1996-12-25 1998-07-07 Lion Corp Oral composition
WO1998030169A1 (en) 1997-01-10 1998-07-16 Ultradent Products, Inc. Stable light or heat activated dental bleaching compositions
US5785527A (en) 1997-01-10 1998-07-28 Ultradent Products, Inc. Stable light or heat activated dental bleaching compositions
US6391283B1 (en) 1997-01-10 2002-05-21 Ultradent Products, Inc. Methods and apparatus for activating dental compositions
US6387353B1 (en) 1997-01-10 2002-05-14 Ultradent Products, Inc. Light or heat activated dental bleaching compositions
US5858332A (en) 1997-01-10 1999-01-12 Ultradent Products, Inc. Dental bleaching compositions with high concentrations of hydrogen peroxide
WO1998033761A1 (en) 1997-01-30 1998-08-06 Ciba Specialty Chemicals Holding Inc. Non-volatile phenylglyoxalic esters
JP2001511137A (en) 1997-01-30 2001-08-07 チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド Non-volatile phenylglyoxylate
US6337357B1 (en) 1997-02-24 2002-01-08 Kuraray Co., Ltd. Antimicrobial caries-detecting composition
US6084005A (en) 1997-02-24 2000-07-04 Kuraray Co., Ltd. Antimicrobial caries-detecting composition
US5922331A (en) 1997-03-26 1999-07-13 Chanel, Inc. Skin cream composition
JPH10330235A (en) 1997-06-02 1998-12-15 Lion Corp Denture cleaner
US20020157165A1 (en) * 1997-09-11 2002-10-31 Kroll Mark W. Light selective sports garments
US5914076A (en) * 1997-10-10 1999-06-22 The Glo-Tech Corporation Process for producing longer-lasting, high luminescence, phosphorescent textile fibers
US20080118578A1 (en) 1997-12-11 2008-05-22 Dees H Craig Topical Medicaments and Methods for Photodynamic Treatment of Disease
US7611831B2 (en) * 1998-01-06 2009-11-03 Cerus Corporation Adsorbing pathogen-inactivating compounds with porous particles immobilized in a matrix
WO1999039238A1 (en) 1998-01-28 1999-08-05 Keratoform, Inc. Methods and apparatus for accelerated orthokeratology
JP2002502864A (en) 1998-02-13 2002-01-29 ブライトスマイル, インコーポレイテッド Light activated tooth whitening composition and method of using same
US20030198605A1 (en) 1998-02-13 2003-10-23 Montgomery R. Eric Light-activated tooth whitening composition and method of using same
WO1999040870A1 (en) 1998-02-13 1999-08-19 Britesmile, Inc. Light-activated tooth whitening composition and method of using same
US6162055A (en) 1998-02-13 2000-12-19 Britesmile, Inc. Light activated tooth whitening composition and method of using same
US6343933B1 (en) 1998-02-13 2002-02-05 Britesmile, Inc. Light-activated tooth whitening composition and method of using same
US6149895A (en) 1998-02-17 2000-11-21 Kreativ, Inc Dental bleaching compositions, kits & methods
US5977199A (en) 1998-02-17 1999-11-02 The Kerr Corporation Composition, delivery system therefor, and method for making temporary crowns and bridges
WO1999049823A1 (en) 1998-03-30 1999-10-07 Fibermark, Inc. Light-activated antimicrobial polymeric materials
US6217794B1 (en) * 1998-06-01 2001-04-17 Isotag Technology, Inc. Fiber coating composition having an invisible marker and process for making same
WO1999063900A1 (en) 1998-06-12 1999-12-16 Photogen, Inc. Improved methods and apparatus for multi-photon photo-activation of therapeutic agents
US6036493A (en) 1998-07-23 2000-03-14 Ad Dent Inc. Dental bleaching system and method
US20030085384A1 (en) * 1998-10-13 2003-05-08 Peter Burnell-Jones Heat curable thermosetting luminescent resins
US20050261750A1 (en) 1998-11-30 2005-11-24 Light Bioscience, Llc Method and apparatus for acne treatment
CA2457590A1 (en) 1998-11-30 2003-03-06 Light Bioscience, Llc Method and apparatus for acne treatment
WO2003017824A2 (en) 1998-11-30 2003-03-06 Light Bioscience, Inc. Method and apparatus for acne treatment
US6030222A (en) 1998-12-01 2000-02-29 Tarver; Jeanna G. Dye compositions and methods for whitening teeth using same
CA2360202A1 (en) 1999-01-04 2000-07-13 Richard Rox Anderson Energy activatable material for the treatment of sebaceous gland disorders
WO2000040266A2 (en) 1999-01-04 2000-07-13 The General Hospital Corporation D/B/A Targeting of sebaceous follicles as a treatment of sebaceous gland disorders
US8182473B2 (en) 1999-01-08 2012-05-22 Palomar Medical Technologies Cooling system for a photocosmetic device
US6420455B1 (en) 1999-06-18 2002-07-16 3M Innovative Properties Company Antimicrobial composition containing photosensitizers articles, and methods of use
WO2001000190A2 (en) 1999-06-29 2001-01-04 Fidia Advanced Biopolymers, S.R.L. Hyaluronic acid derivatives for the prevention and treatment of cutaneous scars
US6365134B1 (en) 1999-07-07 2002-04-02 Scientific Pharmaceuticals, Inc. Process and composition for high efficacy teeth whitening
WO2001012181A1 (en) 1999-08-13 2001-02-22 Photogen, Inc. Improved topical medicaments and methods for photodynamic treatment of disease
US20010045677A1 (en) * 1999-09-24 2001-11-29 Kyeng-Jung Kang Phosphorescent fiber and method of manufacturing the same
EP1235544A1 (en) 1999-12-08 2002-09-04 The Procter & Gamble Company Tartar control denture adhesive compositions
US6905672B2 (en) 1999-12-08 2005-06-14 The Procter & Gamble Company Compositions and methods to inhibit tartar and microbes using denture adhesive compositions with colorants
EP1235543A1 (en) 1999-12-08 2002-09-04 The Procter & Gamble Company Tartar control denture adhesive compositions
US6267976B1 (en) 2000-04-14 2001-07-31 Gojo Industries, Inc. Skin cleanser with photosensitive dye
WO2002011539A1 (en) 2000-08-08 2002-02-14 Cytopharm, Inc. Methods and compositions for treating skin ulcers by topical photodynamic therapy
WO2002022097A1 (en) 2000-09-14 2002-03-21 High Tech Laser Method and composition for dental bleaching
US7314470B2 (en) 2000-11-04 2008-01-01 Wolfgang Malodobry Scar-free removal of tattoos
JP2002226349A (en) 2001-01-23 2002-08-14 Addent Inc Dental bleaching composition, activating agent system, and method for applying and activating the dental bleaching composition
US6485709B2 (en) 2001-01-23 2002-11-26 Addent Inc. Dental bleaching gel composition, activator system and method for activating a dental bleaching gel
JP2002233612A (en) 2001-02-07 2002-08-20 Daito Giken:Kk Gable table
JP2002293747A (en) 2001-03-29 2002-10-09 Jinen:Kk Skin preparation for external use
US20030157323A1 (en) * 2001-05-14 2003-08-21 Mikhail Khavkine Hybrid yarns which include oil seed flax plant bast fiber and other fibers and fabrics made with such yarns
US20040147508A1 (en) * 2001-05-30 2004-07-29 Photopharmica Limited Biologically active methylene blue derivatives
WO2003000215A1 (en) 2001-06-21 2003-01-03 Herbariorum Medicaminum Officina Alta Badiae S.N.C. Tooth-paste composition having anti-plaque properties
US7066941B2 (en) 2001-07-09 2006-06-27 Perricone Nicholas V Apparatus for skin treatment
US7354448B2 (en) 2001-11-29 2008-04-08 Palomar Medical Technologies, Inc. Dental phototherapy methods and compositions
WO2003061696A2 (en) 2002-01-23 2003-07-31 Light Sciences Corporation Systems and methods for photodynamic therapy
US7081128B2 (en) 2002-03-04 2006-07-25 Hart Barry M Phototherapy device and method of use
WO2003086215A1 (en) 2002-04-11 2003-10-23 Light Bioscience, Inc. Low intensity light therapy for the manipulation of fibroblast-derived mammalian cells and collagen
WO2003099247A1 (en) 2002-05-23 2003-12-04 The Procter & Gamble Company Tooth whitening products
US20080058689A1 (en) 2002-06-12 2008-03-06 University Of Florida Research Foundation, Inc. Phototherapy bandage
US20050098766A1 (en) 2002-09-19 2005-05-12 Watson David L.Jr. Chemiluminescent processes and systems
WO2004028498A1 (en) 2002-09-24 2004-04-08 The Boots Company Plc Dental compositions and methods
US20040136971A1 (en) 2002-10-11 2004-07-15 David Scharp Implantation of encapsulated biological materials for treating diseases
WO2004081222A2 (en) 2003-03-14 2004-09-23 Sol-Gel Technologies Ltd. Agent-encapsulating micro- and nanoparticles, methods for preparation of same and products containing same
US20060251687A1 (en) 2003-03-14 2006-11-09 Noa Lapidot Agent-encapsulating micro-and nanoparticles, methods for preparation of same and products containing same
US20040191330A1 (en) 2003-03-31 2004-09-30 Keefe Candace R. Daily skin care regimen
WO2004104277A1 (en) 2003-05-22 2004-12-02 Landqart Photoluminescent fibre, security paper and other security articles
JP2003339875A (en) 2003-06-16 2003-12-02 Hirokatsu Kimura Tatoo eliminating device
US20050123588A1 (en) 2003-06-16 2005-06-09 Zhu Yong H. Deployable multifunctional hemostatic agent
US20040262569A1 (en) 2003-06-24 2004-12-30 Lg.Philips Lcd Co., Ltd. Etchant for etching double-layered copper structure and method of forming array substrate having double-layered copper structures
WO2005009604A1 (en) 2003-07-31 2005-02-03 Sol-Gel Technologies Ltd. Microcapsules loaded with active ingredients and a method for their preparation
US20050026298A1 (en) 2003-08-01 2005-02-03 Tim Bickett Dye solutions for use in methods to detect the prior evaporation of anhydrous ammonia and the production of illicit drugs
US20080206159A1 (en) 2003-08-04 2008-08-28 Foamix Ltd. Compositions with modulating agents
US20050042712A1 (en) 2003-08-22 2005-02-24 Advanced Medical Optics, Inc. Methods, compositions and instruments to predict antimicrobial or preservative activity
US20050042428A1 (en) * 2003-08-22 2005-02-24 Dean David M. Methods for identity verification using transparent luminescent polymers
US6849330B1 (en) * 2003-08-30 2005-02-01 Milliken & Company Thermoplastic fibers exhibiting durable high color strength characteristics
US20050059731A1 (en) 2003-09-16 2005-03-17 Ceramoptec Industries, Inc. Erythrosin-based antimicrobial photodynamic therapy compound and its use
KR20070017292A (en) 2003-09-16 2007-02-09 세람옵텍 인더스트리스, 인크. Erythrosine-Based Antimicrobial Photodynamic Therapeutic Compounds and Uses thereof
WO2005051305A2 (en) 2003-11-19 2005-06-09 Barnes-Jewish Hospital Enhanced drug delivery
US20050244455A1 (en) * 2004-04-20 2005-11-03 Greenawalt Keith E Surgical prosthesis
US20070244195A1 (en) 2004-05-18 2007-10-18 Burkhart Craig N Treatment methods with peroxides and tertiary amines
CA2551613A1 (en) 2004-05-21 2005-12-01 Tottori University A composition comprising n-acetyl-d-glucosamine for treatment of wound
US20060228320A1 (en) 2004-05-21 2006-10-12 Saburo Minami Agent for therapy or treatment of wound
CA2580381A1 (en) 2004-06-18 2006-01-26 The Ohio State University Research Foundation Methods and compositions for wound healing
WO2006014597A1 (en) 2004-07-08 2006-02-09 3M Innovative Properties Company Dental methods, compositions, and kits including acid-sensitive dyes
US20070149722A1 (en) * 2004-08-05 2007-06-28 General Electric Company Flame retardant thermoplastic polycarbonate compositions, method of manufacture, and method of use thereof
WO2006032847A1 (en) 2004-09-20 2006-03-30 Photopharmica Limited Wound healing
WO2006047868A1 (en) 2004-11-02 2006-05-11 John Kennedy Method of treating microorganisms in the oral cavity via photodynamic therapy employing a non-coherent light source
WO2006072243A1 (en) 2005-01-03 2006-07-13 Novozymes Biopolymer A/S Hyaluronic acid fraction with moisturizing and anti-wrinkle properties
US20060199242A1 (en) 2005-03-01 2006-09-07 Ching-Ying Cheung Chemical probe compounds that become fluorescent upon reduction, and methods for their use
US20080060148A1 (en) * 2005-03-09 2008-03-13 Pinyayev Aleksey M Sensor responsive electric toothbrushes and methods of use
US20060217690A1 (en) 2005-03-22 2006-09-28 Bastin Norman J Method for treating various dermatological and muscular conditions using electromagnetic radiation
WO2006118835A2 (en) 2005-04-29 2006-11-09 Johnson & Johnson Consumers Companies, Inc. Topical composition fluorescence detection
WO2006125650A1 (en) 2005-05-25 2006-11-30 3M Espe Ag Dental composition for detection of carious tissue, detection method
WO2006135344A1 (en) 2005-06-13 2006-12-21 National University Of Singapore A photosensitising composition and uses thereof
JP2009500135A (en) 2005-07-14 2009-01-08 サンソウル インコーポレーテッド Protective materials, items and protective methods
US20070016173A1 (en) * 2005-07-14 2007-01-18 Michael Kreindel Protective material, clothing item and method of protection
US20070021807A1 (en) 2005-07-20 2007-01-25 Eastman Kodak Company Device for optically stimulating collagen formation in tissue
US20080255498A1 (en) * 2005-08-25 2008-10-16 Houle Philip R Sensitizer Solutions, Systems, and Methods of Use
WO2007025244A2 (en) 2005-08-25 2007-03-01 Houle Philip R Treatment systems for delivery of sensitizer solutions
US20070092469A1 (en) 2005-10-26 2007-04-26 Eric Jacobs Topically applied Glucosamine Sulfate and all its related, precursor, and derivative compounds significantly increases the skin's natural produciton of hyaluronic acid for the rejuvenation of healthier younger-looking skin; while PhosphatidylCholine is required to replace its deficiency caused by topical Dimethylaminoethanol (DMAE)
EP1779891A1 (en) 2005-10-28 2007-05-02 Abdula Kurkayev Method of activating a photosensitizer
US20120171641A1 (en) 2005-11-09 2012-07-05 Klox Technologies Inc. Teeth whitening composition and methods
EP1951184A2 (en) 2005-11-09 2008-08-06 Picchio International Inc. Teeth whitening compositions and methods
US8986719B2 (en) 2005-11-09 2015-03-24 Klox Technologies Inc. Teeth whitening compositions and methods
US20150290103A1 (en) 2005-11-09 2015-10-15 Klox Technologies Inc. Teeth whitening compositions and methods
WO2007080453A2 (en) 2005-11-09 2007-07-19 Klox Technologies Inc. Teeth whitening compositions and methods
EP2338465A1 (en) 2005-11-09 2011-06-29 Klox Technologies Inc. Teeth whitening compositions and methods
US8075875B2 (en) 2005-11-09 2011-12-13 Klox Technologies Inc. Teeth whitening composition and methods
US20070128132A1 (en) 2005-11-09 2007-06-07 Remigio Piergallini Teeth whitening composition and methods
US20070142762A1 (en) * 2005-12-16 2007-06-21 Eastman Kodak Company Wound dressing
US20080262154A1 (en) * 2005-12-22 2008-10-23 Basf Se Aqueous Dispersions of Polymers which Comprise a Fluorescent Dye, Process for Their Production and Their Use for Marking Materials
US20070166369A1 (en) 2006-01-18 2007-07-19 Ceramoptec Industries, Inc. Photodynamic cosmetic procedure and healing method
WO2007087259A2 (en) 2006-01-23 2007-08-02 The Procter & Gamble Company Enzyme and photobleach containing compositions
US20070191249A1 (en) 2006-01-23 2007-08-16 The Procter & Gamble Company Enzyme and photobleach containing compositions
WO2007127172A2 (en) 2006-04-27 2007-11-08 The Trustees Of Columbia University In The City Of New York Layered bio-adhesive compositions and uses thereof
US20070288071A1 (en) * 2006-06-07 2007-12-13 Rogers Gary S Continuous low irradiance photodynamic therapy system and method
US20070290172A1 (en) * 2006-06-19 2007-12-20 General Electric Company Infrared transmissive thermoplastic composition, and articles formed therefrom
US20100063467A1 (en) * 2006-07-13 2010-03-11 Deborah Addison Hydrogel Wound Dressings Exhibiting Reduced Fiber Losses in Use
WO2008011707A1 (en) 2006-07-24 2008-01-31 Quest Pharmatech Inc. Method and device for photodynamic therapy
WO2008013962A2 (en) 2006-07-28 2008-01-31 Ceramoptec Industries, Inc. Method and mixture for in-vivo photochemical cross-linking of collagen
WO2008052081A2 (en) 2006-10-24 2008-05-02 California Institute Of Technology Photochemical therapy to affect mechanical and/or chemical properties of body tissue
US20080108681A1 (en) 2006-10-27 2008-05-08 Access Business Group International Llc Use of allantoin as a pro-collagen synthesis agent in cosmetic compositions
US20130122467A1 (en) 2006-11-09 2013-05-16 Klox Technologies Inc. Photoactivatable oxygen-evolving compositions and methods for teeth whitening
US20100266989A1 (en) 2006-11-09 2010-10-21 Klox Technologies Inc. Teeth whitening compositions and methods
US20080113037A1 (en) 2006-11-10 2008-05-15 Green Barbara A Topical Compositions Comprising Polyhydroxy Acids and/or Lactones for Improved Cutaneous Effects of Oxidative Therapeutic Drugs
US20080138289A1 (en) 2006-12-08 2008-06-12 Evident Technologies, Inc. Systems and methods for detecting infrared emitting composites and medical applications therefor
US20100040809A1 (en) * 2006-12-27 2010-02-18 Mueller Daniel Multifilament, monofilament, non-woven or tape
US20080305101A1 (en) 2007-01-03 2008-12-11 Erkki Ruoslahti Methods and Compositions Related to Clot Binding Compounds
US20090036593A1 (en) * 2007-07-31 2009-02-05 Sabic Innovative Plastics Ip Bv Polycarbonate compositions with improved molding capability
US20090041984A1 (en) * 2007-08-10 2009-02-12 Nano Terra Inc. Structured Smudge-Resistant Coatings and Methods of Making and Using the Same
US20100255045A1 (en) 2007-11-27 2010-10-07 Eymard Du Vernet Michele Composition for photodynamic skin treatment
CA2706808A1 (en) 2007-11-27 2009-08-06 Michele Eymard Du Vernet Composition for photodynamic skin treatment
WO2009089346A2 (en) 2008-01-08 2009-07-16 Quick-Med Technologies, Inc. Disinfectant alcohol-soluble quaternary ammonium polymers
US20140309717A1 (en) * 2008-01-16 2014-10-16 Morgan Lars Ake Gustavsson Fluorescent handpiece
US20090246251A1 (en) * 2008-03-27 2009-10-01 Affinergy Coating compositions having improved performance
GB2469219A (en) * 2008-04-10 2010-10-06 Kythera Biopharmaceuticals Inc Dermal filler composition
CA2738035A1 (en) 2008-09-29 2010-04-01 Mallinckrodt Inc. Dithienopyrrole dyes for imaging and therapy
US20110245748A1 (en) 2008-10-01 2011-10-06 Action Bandage, Llc Wound care device
CA2742942A1 (en) 2008-11-07 2010-05-14 Klox Technologies Inc. Combination of an oxidant and a photoactivator for the healing of wounds
WO2010051636A1 (en) 2008-11-07 2010-05-14 Klox Technologies Inc . Combination of an oxidant and a photoactivator for the healing of wounds
US8632822B2 (en) 2008-11-07 2014-01-21 Klox Technologies Inc. Combination of an oxidant and a photoactivator for the healing of wounds
US8658219B2 (en) 2008-11-07 2014-02-25 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US8911791B2 (en) 2008-11-07 2014-12-16 Klox Technologies Inc. Method for acne treatment using an oxidative-photoactivated composition
US8637086B2 (en) 2008-11-07 2014-01-28 Klox Technologies Inc. Method for acne treatment using an oxidative-photoactivated composition
US20150065453A1 (en) 2008-11-07 2015-03-05 Klox Technologies Inc. Combination of an oxidant and a photoactivator for the healing of wounds
US9375446B2 (en) 2008-11-07 2016-06-28 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US8974833B2 (en) 2008-11-07 2015-03-10 Klox Technologies Inc. Combination of an oxidant and a photoactivator for the healing of wounds
WO2010051641A1 (en) 2008-11-07 2010-05-14 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US8986745B2 (en) 2008-11-07 2015-03-24 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
CA2742943A1 (en) 2008-11-07 2010-05-14 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US20150306131A1 (en) 2008-11-07 2015-10-29 Klox Technologies Inc. Oxidatitive photoactivated skin rejeuvenation composition comprising hyaluronic acid, glucosamine, or allantoin
US20100125963A1 (en) * 2008-11-21 2010-05-27 E. I. Du Pont De Nemours And Company Monofilament comprising hydrophilic agent
JP2012512932A (en) 2008-12-19 2012-06-07 キンバリー クラーク ワールドワイド インコーポレイテッド Plasticizers for thermoplastic polymer materials
US20100159769A1 (en) * 2008-12-19 2010-06-24 Macdonald John G Plasticizer for thermoplastic materials
WO2010070292A1 (en) 2008-12-20 2010-06-24 Convatec Technologies Inc A composition for use on skin and wound
CA2745059A1 (en) 2008-12-20 2010-06-24 Convatec Technologies Inc. Photo-catalyst compositions for diagnosis and treatment of biofilms in wounds
US20100227799A1 (en) 2009-03-09 2010-09-09 Medtronic Vascular, Inc. Simultaneous photodynamic therapy and photo induced polymerization
WO2010151563A1 (en) 2009-06-25 2010-12-29 3M Innovative Properties Company Light-activated antimicrobial article and method of use
US20120100039A1 (en) * 2009-06-25 2012-04-26 Appeaning Maria A Light-activated antimicrobial article and method of use
US8986746B2 (en) 2009-07-17 2015-03-24 Klox Technologies Inc. Combination of an oxidant, a photosensitizer and a wound healing agent for oral disinfection and treatment of oral disease
WO2011006263A1 (en) 2009-07-17 2011-01-20 Klox Technologies Inc. Antibacterial oral composition
US20150290320A1 (en) 2009-07-17 2015-10-15 Klox Technologies Inc. Combination of an oxidant, a photosensitizer and a wound healing agent for oral disinfecton and treatment of oral disease
US8685466B2 (en) 2009-07-17 2014-04-01 Klox Technologies Inc. Combination of an oxidant, a photosensitizer and a wound healing agent for oral disinfection and treatment of oral disease
JP2011063889A (en) 2009-09-15 2011-03-31 Fujifilm Corp Cross-spray electric field spinning
WO2011058448A2 (en) 2009-10-27 2011-05-19 Klox Technologies Inc. Device for personal use in phototherapy
US20120283622A1 (en) * 2009-11-10 2012-11-08 Nath Guenther Dermatological treatment device
US20110143621A1 (en) * 2009-12-10 2011-06-16 Macdonald John Gavin Plasticizer for thermoplastic polymer materials
US20110171310A1 (en) 2010-01-13 2011-07-14 Allergan Industrie, Sas Hydrogel compositions comprising vasoconstricting and anti-hemorrhagic agents for dermatological use
US20130115843A1 (en) * 2010-04-23 2013-05-09 Pegas Nonwovens S.R.O. Method of producing a nonwoven textile comprising a barrier and an antistatic treatment
WO2011134087A1 (en) 2010-04-30 2011-11-03 Klox Technologies Inc. Photoactivatable oxygen-evolving compositions and methods for teeth whitening
US20110313407A1 (en) * 2010-06-18 2011-12-22 Rafailov Edik U Quantum-dot laser diode
CA2809405A1 (en) 2010-07-21 2012-01-26 Republic Polytechnic Compounds for photodynamic therapy
WO2012011875A1 (en) 2010-07-21 2012-01-26 Republic Polytechnic Compounds for photodynamic therapy
US20120080613A1 (en) * 2010-09-30 2012-04-05 Performance Indicator, Llc. Photolytically and Environmentally Stable Multilayer Structure for High Efficiency Electromagnetic Energy Conversion and Sustained Secondary Emission
US20120116391A1 (en) * 2010-11-05 2012-05-10 Houser Kevin L Surgical instrument with sensor and powered control
WO2012072980A1 (en) 2010-11-30 2012-06-07 Convatec Technologies Inc A composition for detecting biofilms on viable tissues
US20120157576A1 (en) * 2010-12-16 2012-06-21 Ticona Llc Polyoxymethylene Fibers in Concrete
CN102603232A (en) 2010-12-16 2012-07-25 提克纳有限责任公司 Polyoxymethylene fibers in concrete
CN102133208A (en) 2011-03-17 2011-07-27 北京化工大学 Photosensitive microcapsule used for photodynamic therapy and preparation method thereof
US20140308867A1 (en) * 2011-04-19 2014-10-16 Ar Metallizing N.V. Antimicrobial nonwoven fabric
US20130060183A1 (en) * 2011-09-02 2013-03-07 John Cuevas Ramirez Attachable grip enhancers and uses and methods of said enhancers
US20140306869A1 (en) * 2011-09-21 2014-10-16 Sharp Kabushiki Kaisha Transition metal complex having alkoxy group, organic light-emitting device using same, color conversion light-emitting device using same, light conversion light-emitting device using same, organic laser diode light-emitting device using same, dye laser using same, display system using same, lighting system using same, and electronic equipment using same
US20140082859A1 (en) * 2011-12-21 2014-03-27 Shaw Industries Group, Inc. System and method for space-dyeing yarn
WO2013113349A1 (en) 2012-01-30 2013-08-08 Merck Patent Gmbh Nanocrystals on fibers
JP2015510668A (en) 2012-01-30 2015-04-09 メルク パテント ゲーエムベーハー Nanocrystals on fiber
US20130281913A1 (en) 2012-04-20 2013-10-24 Klox Technologies Inc. Biophotonic compositions and methods for providing biophotonic treatment
WO2013155620A1 (en) 2012-04-20 2013-10-24 Klox Technologies Inc. Biophotonic compositions, kits and methods
US20150246127A1 (en) 2012-04-20 2015-09-03 Klox Technologies Inc. Chromophore Combinations for Biophotonic Uses
US20150119788A1 (en) 2012-04-20 2015-04-30 Klox Technologies Inc. Biophotonic compositions, kits and methods
CA2868893A1 (en) 2012-04-20 2013-10-24 Klox Technologies Inc. Biophotonic compositions, kits and methods
US20150360047A1 (en) 2012-09-14 2015-12-17 Klox Technologies Inc. Cosmetic Biophotonic Compositions
US20140105832A1 (en) * 2012-09-14 2014-04-17 Valeant Pharmaceuticals International, Inc. Compositions and methods for teeth whitening
US20160136075A1 (en) 2012-09-14 2016-05-19 Valeant Pharmaceuticals International, Inc. Compositions and methods for teeth whitening
JP2015528472A (en) 2012-09-14 2015-09-28 クロックス テクノロジーズ インコーポレイテッドKlox Technologies Inc. Chromophore combinations for biophotonic use
WO2014040176A1 (en) 2012-09-14 2014-03-20 Klox Technologies Inc. Chromophore combinations for biophotonic uses
WO2014040177A1 (en) 2012-09-14 2014-03-20 Klox Technologies Inc. Cosmetic biophotonic compositions
US20140128943A1 (en) * 2012-11-07 2014-05-08 Rogers Sciences, Inc. Implantable clipt illumination system
US20140161850A1 (en) 2012-12-11 2014-06-12 Elc Management Llc Cosmetic Compositions With Near Infra-Red (NIR) Light - Emitting Material And Methods Therefor
JP2016505553A (en) 2012-12-11 2016-02-25 イーエルシー マネージメント エルエルシー Cosmetic composition having near-infrared (NIR) luminescent material and method thereof
US20140303547A1 (en) 2013-03-01 2014-10-09 Klox Technologies Inc. Phototherapeutic device, method and use
US20140260437A1 (en) * 2013-03-13 2014-09-18 Robert H. Fleming, Jr. Skin-Contacting Tubular Fabric Underlay For Use Beneath A Therapeutic or Prosthetic Device
CA2902363A1 (en) * 2013-03-14 2014-09-18 Klox Technologies Inc. Biophotonic materials and uses thereof
JP2016514000A (en) 2013-03-14 2016-05-19 クロックス テクノロジーズ インコーポレイテッドKlox Technologies Inc. Biophotonic material and use thereof
WO2014138930A1 (en) 2013-03-14 2014-09-18 Klox Technologies Inc. Biophotonic materials and uses thereof
US20140276354A1 (en) 2013-03-14 2014-09-18 Klox Technologies Inc. Biophotonic materials and uses thereof
WO2015000058A1 (en) 2013-07-03 2015-01-08 Klox Technologies Inc. Biophotonic compositions comprising a chromophore and a gelling agent for treating wounds
WO2015184551A1 (en) 2014-06-04 2015-12-10 Klox Technologies Inc. Biophotonic hydrogels
US20170209348A1 (en) * 2014-06-24 2017-07-27 Klox Technologies Inc. Biophotonic compositions comprising halogen and uses thereof
WO2016065488A1 (en) 2014-10-31 2016-05-06 Klox Technologies Inc. Photoactivatable fibers and fabric media
US20160205925A1 (en) * 2015-01-15 2016-07-21 Ariel-University Research And Development Company Ltd. Antimicrobial compositions made of a thermoplastic polymer and a photosensitizer
WO2017201615A1 (en) 2016-05-23 2017-11-30 Orphaderm Limited Biophotonic compositions comprising a fungal-derived chromophore
US20200063299A1 (en) * 2016-11-01 2020-02-27 Teijin Limited Fabric, method for manufacturing same, and fiber product

Non-Patent Citations (63)

* Cited by examiner, † Cited by third party
Title
Alster, et al., "Photodynamic therapy: practical cosmetic applications," Journal of Drugs in Dermatology, 5(8):764-768 (2006).
Antunes, et al., "Evaluation of the ciastogenicity and anticiastongenicity of the carotenoid bixin in human lymphocyte cultures," Mutation Research, 585(1-2):113-9 (2005).
Ariizumi et al., "Clinical evaluation of a topical applicant TSG-88 for periodontal disease," Dental Drug Therapy, 10(2):157-168 (1991) (English Abstract included).
Berneburg, et al., "Phototherapy with narrowband UVB," Acta Dermato-Venereologica, 85:1-11 (2005).
CARLOS VAN HEMELRIJCK, CHRISTEL C. MÜLLER-GOYMANN: "Rheological characterization and permeation behavior of poloxamer 407-based systems containing 5-aminolevulinic acid for potential application in photodynamic therapy", INTERNATIONAL JOURNAL OF PHARMACEUTICS, ELSEVIER, NL, vol. 437, no. 1-2, 1 November 2012 (2012-11-01), NL , pages 120 - 129, XP055419977, ISSN: 0378-5173, DOI: 10.1016/j.ijpharm.2012.07.048
Chen et al., "Study of the chemiluminescent characteristics of some xanthone dyes," Analytica Chimica Acta, 292(1-2):159-167 (1994).
Clark, et al., "Eosin-Phloxine alcoholic solution," Mitt. Zool. Stat. Neapel, Jan. 1, 1981 (Jan. 1, 1981), pp. 170-186, XP055224968, Retrieved from the Internet: URL:http://tunic.ro/fise/tehnice/05-10020L.pdf * abstract * (1 page).
Colman, et al., "The healing of wounds in the skin of piglets treated with benzoyl peroxide," The Journal of Dermatologic Surgery and Oncology, 4(9):705-707 (1978).
Darzynkiewicz, et al., "Photosensitizing effects of the tricyclic heteroaromatic cationic dyes Pyronin Y and Toluidine Blue O (tolonium chloride)," Cancer Research, 48(5):1295-1299 (1988).
DATABASE GNPD [online] MINTEL; 1 May 2007 (2007-05-01), "Active Plus Deep Cleaning Tablets", XP002769877
DATABASE GNPD [online] MINTEL; 1 May 2009 (2009-05-01), "Effervescent Tablets", XP002769876
DATABASE GNPD [online] MINTEL; 30 November 2010 (2010-11-30), ANONYMOUS: "Photo dynamic therapy SPF 30", XP002775115
De, et al., "Environmental effects on the aggregation of some xanthene dyes used in lasers," Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 61(8):1821-1833 (2005).
Decraene et al., "Cellulose acetate containing Toluidine Blue and Rose Bengal is an effective antimicrobial coating when exposed to white light," Applied and Env. Microbiology, 72:6(4436-4439) (Jun. 2006).
Dumortier, et al., "A Review of Poloxamer 407; Pharmaceutical and Pharmacological Characteristics",; Pharmaceutical Research, Kluwer Academic Publishersplenum Publishers. NL,; vol. 23, No. 12, 11, pp. 2709-2728, XP019453318, ISSN: 1573-904X, DOI: 1 0.1 007/811 095-006-91 04-4 (Nov. 2006).
English abstract provided for CN 102603232 A.
Eurasian Search Report, Serial No. 201291068, dated May 29, 2013 with English translation (3 pages).
European Supplementary Search Report, Application No. EP09824320, dated Mar. 28, 2012 (12 pages).
FDA, Color Additive Status List, http://www.cfsanJda.gov/-dms/opa-appc.html, downloaded Jun. 18, 2008 (13 pages).
FDA, Product Classification Database Search, http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpcd/classificiation/c.f?ID-3964, Device: Eosin y: database, downloaded Jun. 18, 2008 (2 pages).
Fisher Scientific, "Material Safety Data Sheet: Sodium acetate buffer," https://fscimagef.fishersci.com/msds/91502.htm (ACC #91502) (Apr. 13, 2000) (5 pages).
G CLARK, WILLIAMS, II WILKINS, P MAYER: "Eosin-Phloxine alcoholic solution", MITT. ZOOL. STAT. NEAPEL, 1 January 1981 (1981-01-01), pages 170 - 186, XP055224968, Retrieved from the Internet <URL:http://tunic.ro/fise/tehnice/05-10020L.pdf>
GILLES DUMORTIER ; JEAN LOUIS GROSSIORD ; FLORENCE AGNELY ; JEAN CLAUDE CHAUMEIL: "A Review of Poloxamer 407 Pharmaceutical and Pharmacological Characteristics", PHARMACEUTICAL RESEARCH, KLUWER ACADEMIC PUBLISHERS-PLENUM PUBLISHERS, NL, vol. 23, no. 12, 11 November 2006 (2006-11-11), NL , pages 2709 - 2728, XP019453318, ISSN: 1573-904X, DOI: 10.1007/s11095-006-9104-4
Goldberg, "Photodynamic therapy in skin rejuvenation," Clinics in Dermatology, 26(6):608-613 (2008).
Gonzales et al., "Photodynamic inactivation of microorganisms as an innovative approach to kill mucocutaneous and skin microorganisms," Giornale Italiano Di Dermatologia e Venereologia, 145, pp. 477-489 (2010).
Jankowski, et al., "The action of photosensitizers and serum in a bactericidal process. II. The effects of dyes: Hypericin, Eosin Y and Saphranine O," Polish Journal of Microbiology, 54(4):323-330 (2005).
Kelly, et al., "Combined photodynamic and photothermal induced injury enhances damage to in vivo model blood vessels," Lasers in Surgery and Medicine, 34(5):407-413 (2004).
Korb, et al., "An evaluation of the efficacy of Fluorescein, Rose Bengal, Lissamine Green, and a new dye mixture for ocular surface staining," Eye Contact Lens, Jan. 2008;34(1) 61-64. Jan. 1, 2008 (Jan. 1, 2008), XP055224976, Retrieved from the Internet: URL:http://www.ncbi.nlm.nih.gov/pubmed/181 80687 [retrieved on Nov. 2, 2015] * abstract * (1 page).
Lins, et al., "Enhancement of Antimicrobial Action of Photodynamic Therapy in the Presence of Hydrogen Peroxide," in Microbial Pathogens and Strategies for Combating Them: Science, Technology and Education, Edition: Microbiology Book Series #4, Editor: A. Mendez-Vilas, pp. 367-371 (2013) (acquired from:; https://www.researchgate.net/publication/283644315_Enhancement of Antimicrobial_Action_of_Photodynamic_Therapy_in_the_Presence_of; Hydrogen_Peroxide).
Mao, Kailiang, "Listen to Chemical Anecdotes", Distant Press, p. 219, paragraph 1 and p. 220, paragraph 3, Aug. 2007.
McCullach, et al., "Photosensitized destruction of Chtoreiia vulgaris by Methylene Blue or Nuclear Fast Red combined with hydrogen peroxide under visible light irradiation," Environmental Science and Technology, 40(7):2421-2425 (2006).
Meisel, et al., "Photodynamic therapy for periodontal diseases: state of the art," Journal of Photochemistry and Photobiology B: Biology, 79:159-170 (2005).
Mintel, "Active Plus Deep Cleaning Tablets," Database GNPD [Online].; May 2007, XP002769877, Database accession No. 707777 *Ingredients*.
Mintel, "Effervescent Tablets," Database GNPD [Online] ; May 2009, XP002769876, Database accession No. 1089966 *Ingredients*.
Mintel, "Gel Blush," http://gnpd.com; Jun. 2009 (4 pages).
Mintel, "Gold Bear Gums," http://gnpd.com, Feb. 2008 (3 pages).
Mintel, "Photo dynamic therapy SPF 30"XP002775115.; Database accession No. 1442681, pp. 1.2.3.5 (Nov. 30, 2010).
Mintel, "Teens Braces Cleaner," http://gnpd.com, Jan. 2004 (2 pages).
Mintel, "Velvet Gloss Lip Pencil," http://gnpd.com; Feb. 2011 (4 pages).
Montenegro, et al., "Model studies on the photosensitized isomerization of bixin," Journal of Agriculture and Food Chemistry, 52(2): 367-73 (2004).
Nolan et al., "The efficacy of topical hyaluronic acid in the management of oral lichen planus," Journal of Oral Pathology and Medicine, 38(3):299-303 (2006).
Olympus America Inc., "Special characteristics of common biological stains," http://micro.magnet.fsu.edu/primer/photomicrography/bwstainchart.html, Apr. 30, 2000 (3 pages).
PCT international Preliminary Report on Patentability and Written Opinion for international Application No. PCT/CA2013/000787, dated Nov. 27, 2013 (9 pages).
PCT International Search Report and Written Opinion for International Application No. PCT/CA2013/000786, dated Jan. 8, 2014 (16 pages).
PCT International Search Report and Written Opinion for International Application No. PCT/CA2015/000407, dated Sep. 23, 2015 (13 pages).
PCT International Search Report Corrected for international Application No. PCT/CA2014/000261, dated Jul. 23, 2014 (7 pages).
PCT International Search Report for International Application No. PCT/CA2009/001615, dated Feb. 9, 2010 (9 pages).
PCT International Search Report for International Application No. PCT/CA2010/001134, dated Oct. 8, 2010 (3 pages).
PCT International Search Report for International Application No. PCT/CA2013/000395, dated Jul. 15, 2013 (12 Pages).
PCT International Search Report for International Application No. PCT/CA2014/000536, dated Oct. 16, 2014 (7 pages).
Publication date of following document established by Internet Archive Wayback Machine (3 pages) <URL: <http://web.archive.Org/web/20090208211504/http://en.wikipedia.org/wiki/Eosin Aug. 2, 2009.
Resources: Fluorochrome absorption emission wavelengths, [Online] XP002449595 Retrieved from the Internet: URL: http://www.sciencegateway.org/resource s/fae1.htm> retrieved on Sep. 6, 2007] see p. 2: Rhodamine WT emission nm 555 p. 2 (12 pages).
Roy, et al., "Dermal wound healing is subject to redox control," Molecular Therapy, 13(1):211-220 (2006).
Sezer, et al., "Topical drug delivery using chitosan nano- and microparticles," Expert Opinion in Drug Delivery, Informa UK, 9(9):1129-1146 (2012).
Siyusareva, et al. "Spectral and Photophysical Properties of Flourone Dyes in Bio-Related Films and Methanol", Journal of Photochemistry and Photobiology A; Chemistry 208 (2009), pp. 131-140.
Steinberg, et al., "Genetic and physiological effects of noncoherent visible light combined with hydrogen peroxide on Streptococcus mutans in biofilm," Antimicrobial Agents and Chemotherapy, 52(7):2626-2631 (2008).
Subba, et al., "Photocataiytic transformation of dyes and by-products in the presence of hydrogen peroxide," Environmental Technology, 24(8):1025-1030 (2003).
Sun, "Lasers and light amplification in dentistry," retrieved online at http://www.sundds.comllaser/, downloaded Jun. 23, 2005 (14 pages).
Supplementary European Search Report of European Patent Application No. 15855982.3, dated Apr. 3, 2018; Munich, Anna Kajzar.
Tao, et al., "Gastrointestinal Patch Systems for Oral Drug Delivery", Drug Discovery Today, vol. 10, No. 13, Jul. 2005, pp. 909-915.
Thompson, et al., "Fluorescence polarization standards for high-throughput screening and imaging," Bio Techniques, 32(2002) (5 pages).
Tsuboi et al., "Photoluminescence Properties of Fluorone Dyes in Bio-Related Films at Low Temperatures" Journal of Photochemistry and Photobiology A; Chemistry; 222 (2011) pp. 336-342.
Van Hemelrijck, et al., "Rheological characterization and permeation behavior of poloxamer 407-based systems containing 5-arinolevulinic acid for potential application in photodynamic therapy", International Journal of Pharmaceutics,: vol. 437, No. 1-2, Nov. 1, 2012 (Nov. 1, 2012), pp. 120-129,; XP055419977, Amsterdam,NL ISSN: 0378-5173, DOI: 10.1016/j.ijpharm.2012.07.048.

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11998759B2 (en) 2018-08-21 2024-06-04 Lumia Group, LLC Electrically passive low-level light therapy system and methods incorporating same

Also Published As

Publication number Publication date
EP3212826A4 (en) 2018-05-23
AU2015337786A1 (en) 2017-05-25
MX2017005673A (en) 2017-08-02
AR102493A1 (en) 2017-03-01
US20170362744A1 (en) 2017-12-21
EP3212826B1 (en) 2020-10-14
AU2015337786B2 (en) 2020-03-26
CA2966010C (en) 2023-04-11
BR112017008849B1 (en) 2022-05-24
WO2016065488A1 (en) 2016-05-06
CN107075738B (en) 2021-05-07
ES2856841T3 (en) 2021-09-28
IL252012A0 (en) 2017-06-29
MX380590B (en) 2025-03-12
JP2018500468A (en) 2018-01-11
RU2017117187A (en) 2018-11-30
KR20170077153A (en) 2017-07-05
EP3212826A1 (en) 2017-09-06
CA2966010A1 (en) 2016-05-06
BR112017008849A2 (en) 2017-12-19
JP2021105245A (en) 2021-07-26
CN107075738A (en) 2017-08-18

Similar Documents

Publication Publication Date Title
US11421349B2 (en) Photoactivatable fibers and fabric media
US20200085625A1 (en) Absorbent biophotonic devices and systems for wound healing
Yu et al. Strategies for sustained drug release from electrospun multi‐layer nanostructures
US11633366B2 (en) Delivery systems
CN108265400B (en) A kind of preparation method of flexible white fluorescent nanofiber membrane
US20210228720A1 (en) Absorbent biophotonic fiber system
US20150177423A1 (en) Opto textile
CN111676532A (en) A kind of light-emitting fiber, its preparation method and application, light-emitting mask
Enculescu et al. Influence of morphology on the emissive properties of dye-doped PVP nanofibers produced by electrospinning
US20220273798A1 (en) Inert polymer-coated biophotonic systems
KR102250407B1 (en) Medical Radiation Shielding Fiber and medical blood-sucking pad using the same
HK1242746A1 (en) Photoactivatable fibers and fabric media
HK1242746B (en) Photoactivatable fibers and fabric media
US20230158326A1 (en) Wearable Fabric for Photo-stimulating a Biological System
WO2004043542A1 (en) Electroluminescent textile structure, in particular for medical use
HK40042310A (en) Absorbent biophotonic fiber system
Maisha et al. Light-emitting fabrics for photodynamic therapy
Batory et al. The use of liposomes in the modification of polycaprolactone fibers
EP3789667B1 (en) Side-emitting light guide and method for producing the same
CN115262017A (en) Light-reflecting fiber, light-storing light-reflecting fabric and preparation method thereof

Legal Events

Date Code Title Description
AS Assignment

Owner name: KLOX TECHNOLOGIES INC., CANADA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:PIERGALLINI, REMIGIO;LOUPIS, NIKOLAOS;OHAYON, DAVID;REEL/FRAME:044009/0149

Effective date: 20171017

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

FEPP Fee payment procedure

Free format text: ENTITY STATUS SET TO UNDISCOUNTED (ORIGINAL EVENT CODE: BIG.); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: AWAITING TC RESP., ISSUE FEE NOT PAID

STPP Information on status: patent application and granting procedure in general

Free format text: NOTICE OF ALLOWANCE MAILED -- APPLICATION RECEIVED IN OFFICE OF PUBLICATIONS

STPP Information on status: patent application and granting procedure in general

Free format text: PUBLICATIONS -- ISSUE FEE PAYMENT VERIFIED

STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: FLE INTERNATIONAL S.R.L., ITALY

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:KLOX TECHNOLOGIES INC.;REEL/FRAME:063214/0370

Effective date: 20230215

Owner name: FLE INTERNATIONAL S.R.L., ITALY

Free format text: ASSIGNMENT OF ASSIGNOR'S INTEREST;ASSIGNOR:KLOX TECHNOLOGIES INC.;REEL/FRAME:063214/0370

Effective date: 20230215